You are here: Home / News & Events / News Releases / Dec 11, 2008, NY Firm Recalls Fresh Pork Products...
New York Firm Recalls Fresh Pork Products Due To Possible Dioxin Contamination
Recall Release
CLASS II RECALL
FSIS-RC-049-2008
HEALTH RISK: LOW
Congressional and Public Affairs(202) 720-9113Roger SockmanWASHINGTON, Dec. 11, 2008 - Tommy Moloney's Inc., a Long Island City, NY., establishment, is recalling approximately 4,041 pounds of fresh pork products that may be contaminated with dioxins, the U.S. Department of Agriculture's Food Safety and Inspection Service announced today.FSIS was notified by the Food Safety Authority of Ireland (FSAI) that routine surveillance tests indicated the presence of dioxin in pork products that were sent to multiple importers of record in the United States. FSIS believes the probability of adverse health effects related to consumption of these pork products to be low, and concurs with the conclusions of a risk assessment conducted by FSAI.The products subject to recall include: [View Label, PDF Only]
8-ounce packages of "Tommy Moloney's Traditional Irish Breakfast Bacon, Made from imported Irish Pork." The label bears the establishment number "EST. 33789" inside the U.S. mark of inspection as well as a "sell by" date between "Dec. 15, 2008" and "Jan. 31, 2009."
The pork products were produced in Ireland between Sept. 1 and Dec. 7, 2008, and were then exported to the United States. These products were sent to retail stores in California, Connecticut, Florida, Massachusetts, New Jersey, New York, Massachusetts and Virginia.Consumers and media with questions about the recall should contact company President Bill Colbert at (718) 326-2100.Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day.
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You are here: Home / News & Events / News Releases / Dec 11, 2008, MA Firm Recalls Fresh Pork Products...
Massachusetts Firm Recalls Fresh Pork Products Due To Possible Dioxin Contamination
Recall Release
CLASS II RECALL
FSIS-RC-050-2008
HEALTH RISK: LOW
Congressional and Public Affairs(202) 720-9113Roger SockmanWASHINGTON, Dec. 11, 2008 - Dawn International, an Acton, Mass., establishment, is recalling approximately 33,880 pounds of fresh pork products that may be contaminated with dioxins, the U.S. Department of Agriculture's Food Safety and Inspection Service announced today.FSIS was notified by the Food Safety Authority of Ireland (FSAI) that routine surveillance tests indicated the presence of dioxin in pork products that were sent to multiple importers of record in the United States. FSIS believes the probability of adverse health effects related to consumption of these pork products to be low, and concurs with the conclusions of a risk assessment conducted by FSAI.The products subject to recall include: [View Labels]
30-pound cartons of "DAWN PORK & BACON, PORK LOIN BACK RIBS, PRODUCT OF REPUBLIC OF IRELAND." The shipping label bears the Irish mark of inspection "IRELAND 332 EC."
The pork products were produced in Ireland between Sept. 1 and Dec. 7, 2008, and were then exported to the United States. These products were shipped to distribution centers in Florida.Consumers and media with questions about the recall should contact the Irish Embassy representative Dr. Clare Thorp at (202) 716-2369.Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day.
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Wednesday, December 17, 2008
Tuesday, December 16, 2008
recalling Freshness Choice Brand Steam Mackerel because the product was found to be uneviscerated
Siam Trading Inc. and Gulf Coast Sea Trade Inc. Recall
Freshness Choice Brand Steam Mackerel
Arlington, VA – Siam Trading Inc. and Gulf Coast Sea Trade Inc. are recalling Freshness Choice Brand Steam Mackerel because the product was found to be uneviscerated prior to processing. It was discovered by New York State Department of Agriculture and Markets Food Inspectors during a routine inspection.
This product may be contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food-borne illness. The sale of this type of fish is prohibited under New York State Agriculture and Markets regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of botulism poisoning, Symptoms of botulism include blurred or double vision, general weakness, poor reflexes, difficulty in swallowing and respiratory paralysis.
The recalled Freshness Choice Brand Steam Mackerel comes in an uncoded 8 ounce plastic bag and is a product of Vietnam. Freshness Choice Brand Steam Mackerel was sold nationwide.
No illnesses have been reported to date in connection with this problem. Consumers who have Freshness Choice Brand Steam Mackerel are advised not to eat it and return it to the place of purchase.
Retailers with questions for Siam Trading Inc. may contact the company at 718-381-7816.
Retailers with questions for Gulf Coast Sea Trade Inc. may contact the company at 626-329-0398.
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N.G.A. is the national trade association representing the retail and wholesale grocers that comprise the independent sector of the food distribution industry. An independent retailer is a privately owned or controlled food retail company operating a variety of formats. Most independent operators are serviced by wholesale distributors, while others may be partially or fully self-distributing. Some are publicly traded but with controlling shares held by the family and others are employee owned. Independents are the true “entrepreneurs” of the grocery industry and dedicated to their customers, associates, and communities. N.G.A. members include retail and wholesale grocers, state grocers associations, as well as manufacturers and service suppliers. For more information about N.G.A. and the independent sector of the industry, see the N.G.A. website: www.NationalGrocers.org.
Freshness Choice Brand Steam Mackerel
Arlington, VA – Siam Trading Inc. and Gulf Coast Sea Trade Inc. are recalling Freshness Choice Brand Steam Mackerel because the product was found to be uneviscerated prior to processing. It was discovered by New York State Department of Agriculture and Markets Food Inspectors during a routine inspection.
This product may be contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food-borne illness. The sale of this type of fish is prohibited under New York State Agriculture and Markets regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of botulism poisoning, Symptoms of botulism include blurred or double vision, general weakness, poor reflexes, difficulty in swallowing and respiratory paralysis.
The recalled Freshness Choice Brand Steam Mackerel comes in an uncoded 8 ounce plastic bag and is a product of Vietnam. Freshness Choice Brand Steam Mackerel was sold nationwide.
No illnesses have been reported to date in connection with this problem. Consumers who have Freshness Choice Brand Steam Mackerel are advised not to eat it and return it to the place of purchase.
Retailers with questions for Siam Trading Inc. may contact the company at 718-381-7816.
Retailers with questions for Gulf Coast Sea Trade Inc. may contact the company at 626-329-0398.
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N.G.A. is the national trade association representing the retail and wholesale grocers that comprise the independent sector of the food distribution industry. An independent retailer is a privately owned or controlled food retail company operating a variety of formats. Most independent operators are serviced by wholesale distributors, while others may be partially or fully self-distributing. Some are publicly traded but with controlling shares held by the family and others are employee owned. Independents are the true “entrepreneurs” of the grocery industry and dedicated to their customers, associates, and communities. N.G.A. members include retail and wholesale grocers, state grocers associations, as well as manufacturers and service suppliers. For more information about N.G.A. and the independent sector of the industry, see the N.G.A. website: www.NationalGrocers.org.
Cambrooke Foods Imitation Cream Cheese and Peanot Butter(TM) Spreads in the U.S. Market
Cambrooke Foods Recalls Certain Cambrooke Foods Imitation Cream Cheese and Peanot Butter(TM) Spreads in the U.S. Market
Arlington, VA -- Cambrooke Foods® is announcing a voluntary recall of all batches of the following products:
Cheddar Wizard Low Protein Imitation Cream Cheese (SKU 10310; 8 oz. jar);
Herb & Garlic Low Protein Imitation Cream Cheese (SKU 10308; 8 oz. jar); and
Plain Low Protein Imitation Cream Cheese (SKU 10306; 8 oz. jar).
Cambrooke Foods® is undertaking this voluntary recall as a precaution because for the above-listed Imitation Cream Cheese products, Listeria monocytogenes was detected through routine batch testing of product at a company facility before it was sent to customers. These batches of Imitation Cream Cheese products were destroyed. While no reports of adverse events have been reported with any product shipped to our customers, we are taking the precautionary step to recall all Imitation Cream Cheese products, regardless of batch number.
To be abundantly cautious and proactive, Cambrooke Foods® is also conducting a market withdrawal of all batches of:
Low Protein Peanot Butter™ (SKU 10809; 16 oz. jar).
This product is being withdrawn because it is produced in the same facility and using the same machinery used to produce the Imitation Cream Cheese products. Testing has not confirmed Listeria contamination in any batch of Low Protein Peanot Butter™ nor have any adverse events been reported as a result of its consumption. No other Cambrooke Foods™ product is produced using this machinery.
Cambrooke Foods™ is working directly with the Food and Drug Administration (FDA) to investigate the cause of this contamination. Cambrooke Foods™ has voluntarily suspended manufacture and distribution of these products pending its investigation.
If you have questions or require further information, contact Cambrooke Foods® toll-free 866-456-9776, ext. 1015, or via email at safetyfirst@cambrookefoods.com.
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N.G.A. is the national trade association representing the retail and wholesale grocers that comprise the independent sector of the food distribution industry. An independent retailer is a privately owned or controlled food retail company operating a variety of formats. Most independent operators are serviced by wholesale distributors, while others may be partially or fully self-distributing. Some are publicly traded but with controlling shares held by the family and others are employee owned. Independents are the true “entrepreneurs” of the grocery industry and dedicated to their customers, associates, and communities. N.G.A. members include retail and wholesale grocers, state grocers associations, as well as manufacturers and service suppliers. For more information about N.G.A. and the independent sector of the industry, see the N.G.A. website: http://www.nationalgrocers.org/.
Arlington, VA -- Cambrooke Foods® is announcing a voluntary recall of all batches of the following products:
Cheddar Wizard Low Protein Imitation Cream Cheese (SKU 10310; 8 oz. jar);
Herb & Garlic Low Protein Imitation Cream Cheese (SKU 10308; 8 oz. jar); and
Plain Low Protein Imitation Cream Cheese (SKU 10306; 8 oz. jar).
Cambrooke Foods® is undertaking this voluntary recall as a precaution because for the above-listed Imitation Cream Cheese products, Listeria monocytogenes was detected through routine batch testing of product at a company facility before it was sent to customers. These batches of Imitation Cream Cheese products were destroyed. While no reports of adverse events have been reported with any product shipped to our customers, we are taking the precautionary step to recall all Imitation Cream Cheese products, regardless of batch number.
To be abundantly cautious and proactive, Cambrooke Foods® is also conducting a market withdrawal of all batches of:
Low Protein Peanot Butter™ (SKU 10809; 16 oz. jar).
This product is being withdrawn because it is produced in the same facility and using the same machinery used to produce the Imitation Cream Cheese products. Testing has not confirmed Listeria contamination in any batch of Low Protein Peanot Butter™ nor have any adverse events been reported as a result of its consumption. No other Cambrooke Foods™ product is produced using this machinery.
Cambrooke Foods™ is working directly with the Food and Drug Administration (FDA) to investigate the cause of this contamination. Cambrooke Foods™ has voluntarily suspended manufacture and distribution of these products pending its investigation.
If you have questions or require further information, contact Cambrooke Foods® toll-free 866-456-9776, ext. 1015, or via email at safetyfirst@cambrookefoods.com.
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N.G.A. is the national trade association representing the retail and wholesale grocers that comprise the independent sector of the food distribution industry. An independent retailer is a privately owned or controlled food retail company operating a variety of formats. Most independent operators are serviced by wholesale distributors, while others may be partially or fully self-distributing. Some are publicly traded but with controlling shares held by the family and others are employee owned. Independents are the true “entrepreneurs” of the grocery industry and dedicated to their customers, associates, and communities. N.G.A. members include retail and wholesale grocers, state grocers associations, as well as manufacturers and service suppliers. For more information about N.G.A. and the independent sector of the industry, see the N.G.A. website: http://www.nationalgrocers.org/.
Cambrooke Foods Imitation Cream Cheese and Peanot Butter(TM) Spreads in the U.S. Market
Cambrooke Foods Recalls Certain Cambrooke Foods Imitation Cream Cheese and Peanot Butter(TM) Spreads in the U.S. Market
Arlington, VA -- Cambrooke Foods® is announcing a voluntary recall of all batches of the following products:
Cheddar Wizard Low Protein Imitation Cream Cheese (SKU 10310; 8 oz. jar);
Herb & Garlic Low Protein Imitation Cream Cheese (SKU 10308; 8 oz. jar); and
Plain Low Protein Imitation Cream Cheese (SKU 10306; 8 oz. jar).
Cambrooke Foods® is undertaking this voluntary recall as a precaution because for the above-listed Imitation Cream Cheese products, Listeria monocytogenes was detected through routine batch testing of product at a company facility before it was sent to customers. These batches of Imitation Cream Cheese products were destroyed. While no reports of adverse events have been reported with any product shipped to our customers, we are taking the precautionary step to recall all Imitation Cream Cheese products, regardless of batch number.
To be abundantly cautious and proactive, Cambrooke Foods® is also conducting a market withdrawal of all batches of:
Low Protein Peanot Butter™ (SKU 10809; 16 oz. jar).
This product is being withdrawn because it is produced in the same facility and using the same machinery used to produce the Imitation Cream Cheese products. Testing has not confirmed Listeria contamination in any batch of Low Protein Peanot Butter™ nor have any adverse events been reported as a result of its consumption. No other Cambrooke Foods™ product is produced using this machinery.
Cambrooke Foods™ is working directly with the Food and Drug Administration (FDA) to investigate the cause of this contamination. Cambrooke Foods™ has voluntarily suspended manufacture and distribution of these products pending its investigation.
If you have questions or require further information, contact Cambrooke Foods® toll-free 866-456-9776, ext. 1015, or via email at safetyfirst@cambrookefoods.com.
# # #
N.G.A. is the national trade association representing the retail and wholesale grocers that comprise the independent sector of the food distribution industry. An independent retailer is a privately owned or controlled food retail company operating a variety of formats. Most independent operators are serviced by wholesale distributors, while others may be partially or fully self-distributing. Some are publicly traded but with controlling shares held by the family and others are employee owned. Independents are the true “entrepreneurs” of the grocery industry and dedicated to their customers, associates, and communities. N.G.A. members include retail and wholesale grocers, state grocers associations, as well as manufacturers and service suppliers. For more information about N.G.A. and the independent sector of the industry, see the N.G.A. website: http://www.nationalgrocers.org/.
Arlington, VA -- Cambrooke Foods® is announcing a voluntary recall of all batches of the following products:
Cheddar Wizard Low Protein Imitation Cream Cheese (SKU 10310; 8 oz. jar);
Herb & Garlic Low Protein Imitation Cream Cheese (SKU 10308; 8 oz. jar); and
Plain Low Protein Imitation Cream Cheese (SKU 10306; 8 oz. jar).
Cambrooke Foods® is undertaking this voluntary recall as a precaution because for the above-listed Imitation Cream Cheese products, Listeria monocytogenes was detected through routine batch testing of product at a company facility before it was sent to customers. These batches of Imitation Cream Cheese products were destroyed. While no reports of adverse events have been reported with any product shipped to our customers, we are taking the precautionary step to recall all Imitation Cream Cheese products, regardless of batch number.
To be abundantly cautious and proactive, Cambrooke Foods® is also conducting a market withdrawal of all batches of:
Low Protein Peanot Butter™ (SKU 10809; 16 oz. jar).
This product is being withdrawn because it is produced in the same facility and using the same machinery used to produce the Imitation Cream Cheese products. Testing has not confirmed Listeria contamination in any batch of Low Protein Peanot Butter™ nor have any adverse events been reported as a result of its consumption. No other Cambrooke Foods™ product is produced using this machinery.
Cambrooke Foods™ is working directly with the Food and Drug Administration (FDA) to investigate the cause of this contamination. Cambrooke Foods™ has voluntarily suspended manufacture and distribution of these products pending its investigation.
If you have questions or require further information, contact Cambrooke Foods® toll-free 866-456-9776, ext. 1015, or via email at safetyfirst@cambrookefoods.com.
# # #
N.G.A. is the national trade association representing the retail and wholesale grocers that comprise the independent sector of the food distribution industry. An independent retailer is a privately owned or controlled food retail company operating a variety of formats. Most independent operators are serviced by wholesale distributors, while others may be partially or fully self-distributing. Some are publicly traded but with controlling shares held by the family and others are employee owned. Independents are the true “entrepreneurs” of the grocery industry and dedicated to their customers, associates, and communities. N.G.A. members include retail and wholesale grocers, state grocers associations, as well as manufacturers and service suppliers. For more information about N.G.A. and the independent sector of the industry, see the N.G.A. website: http://www.nationalgrocers.org/.
Friday, November 28, 2008
U.S. Department of Agriculture's Class 1 recall of Dutch Prime Foods' Hamburgers due to E. coli O157:H7 contamination.Dutch Prime Foods, Inc., a Long
Please review the following message from Alan Talarsky, Environmental Scientist 1, Food and Drug Safety Program, DHSS regarding the U.S. Department of Agriculture's Class 1 recall of Dutch Prime Foods' Hamburgers due to E. coli O157:H7 contamination.Dutch Prime Foods, Inc., a Long Branch, New Jersey firm, is recalling approximately 345 pounds of ground beef products because they may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture's Food Safety and Inspection Service announced. The following products are subject to recall:5-pound and 10-pound vacuum sealed plastic bags of "DUTCH PRIME FOODS HAMBURGER." These packages of ground beef were packed in 5- and 10-pound shipping cases which bear the establishment number "EST. 5206" inside the USDA mark of inspection. These ground beef products were produced on Nov. 18 and distributed to restaurants in New Jersey. A photo of the product label is attached above for your reference.The problem was discovered through a routine FSIS sampling procedure. FSIS has received no reports of illnesses associated with consumption of this product. Anyone with signs or symptoms of foodborne illness should consult a medical professional. E. coli O157:H7 is a potentially deadly bacterium that can cause bloody diarrhea, dehydration, and in the most severe cases, kidney failure. The very young, seniors and persons with weak immune systems are the most susceptible to foodborne illness. Consumers and media with questions about the recall should contact company Secretary-Treasurer Ron Orzechowski at (732) 222-0910. No action is required of local health departments at this time for this recall. However, inspectors should take appropriate enforcement action if these products are encountered during routine inspections.
Wednesday, November 19, 2008
Nestlé Prepared Foods Company, a Springville, Utah, establishment, is recalling approximately 879,565 pounds of frozen chicken meals that may contain
Nestlé Prepared Foods Company, a Springville, Utah, establishment, is recalling approximately 879,565 pounds of frozen chicken meals that may contain foreign materials, the U.S. Department of Agriculture's Food Safety and Inspection Service announced today. The following products are subject to recall:9.5-ounce packages of "LEAN CUISINE PESTO CHICKEN WITH BOW TIE PASTA" brand frozen meals. Printed on each side of each package is a production code of "8280595912" as well as a use-by date of "Best Before MAY 2010." 10.5-ounce packages of "LEAN CUISINE CHICKEN MEDITERRANEAN" brand frozen meals. Printed on the side of each package is a production code of "8231595912" or "8241595912" as well as a use-by date of "Best before SEP 2010": a production code of "8263595912," "8269595911" or "8274595912," as well as a use-by date of "Best before OCT 2010": or, a production code of "8291595912" or "8301595912" as well as a use-by date of "Best before NOV 2010." 12.5-ounce packages of "LEAN CUISINE CHICKEN TUSCAN" brand frozen meals. Printed on the side of each package is a production code of "8234595911" and a use-by date of "Best before SEP 2009": a production code of "8253595911" or "8269595912" as well as a use-by date of "Best before OCT 2009": or, a production code of "8292595911" or "8296595911" as well as a use-by date of "Best before NOV 2009." Each package also bears the USDA mark of inspection as well as the establishment number "EST P-9018." The frozen chicken meals were produced on Aug. 18, Aug. 21, Aug. 28, Sept. 9, Sept. 19, Sept. 25, Sept. 30, Oct. 6, Oct. 17-18, Oct. 22 and Oct. 27 and were distributed to retail establishments nationwide. The problem was discovered after the company received consumer complaints and a report of one injury. The company identified the objects as small pieces of hard plastic. FSIS has not received other reports of injury. Anyone concerned about an injury from consumption of the products should consult a medical professional. Media with questions about the recall should contact Company Marketing Communications Manager Roz O'Hearn at (440) 264-5170. Consumers with questions about the recall should contact Nestlé Consumer Services Center at (800) 227-6188.
Seattle's Favorite Gourmet Cookies & Dessert Co. of Tukwila, WA is recalling Orange Cranberry and Banana Nut Muffin Tops because they contain undeclar
1. Seattle's Favorite Gourmet Cookies & Dessert Co. of Tukwila, WA is recalling Orange Cranberry and Banana Nut Muffin Tops because they contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life threatening allergic reaction if they consume these products.Orange Cranberry and Banana Nut Muffin Tops were distributed nationwide to coffee shops, espresso stands, and retail outlets. These products are individually wrapped in clear plastic with a black product card featuring the Seattle's Favorite logo in upper left hand side and contains the product name and ingredient statement. Product may or may not contain an expiration date or best by date. The date is placed on the product at the retail location. These products, regardless of any codes, are subject to this recall.A sample photo of one of these products is attached above for your reference.There have been no illnesses reported to date.During a routine FDA inspection it was discovered that the ingredient statement did not declare milk.Consumers are urged to return these products to point of purchase for a refund. For any further concerns or questions please contact Seattle's Favorite at seattlesfavoritecookies.com or 1-866-203-5588.
Monday, November 17, 2008
CSI, USA, Inc. issued a voluntary nationwide consumer product recall of all lots of 1 ounce (28 g) tubes of 10% Benzoyl Peroxide Acne Cream with the f
CSI, USA, Inc. issued a voluntary nationwide consumer product recall of all lots of 1 ounce (28 g) tubes of 10% Benzoyl Peroxide Acne Cream with the following names: "DG Maximum Strength Acne Medicated Gel" (sold at Dollar General): "Kroger Acne Gel 10% Benzoyl Peroxide Acne Medication" (sold at Kroger): and "Equate: Medicated Acne Gel" (sold at Wal-Mart).Sample photos of each product can be accessed at the following weblink: http://www.fda.gov/oc/po/firmrecalls/photos/csi11_08.htmlThese products are being recalled because samples of the products were found to contain bacteria identified as "Burkholderia Cepacia," formerly known as Pseudomonas Cepacia. After conducting a thorough assessment, the company concluded that the risk of illness in healthy individuals following use of this product is very low. However, there could be an increased health risk of infections for individuals with cuts, scrapes, rashes or other compromised skin conditions: or those with weakened or suppressed immune systems. No consumer adverse health events related to this issue have been reported. No other acne medications sold by Dollar General, Kroger or Wal-Mart are affected by this recall.Consumers should discontinue using the product and may obtain a full refund by mailing the tube, or proof of purchase, to: CSI USA, Inc.170 Commerce WayGallatin, TN 37066Attn: ACNE CREAM RECALLAdditional information can be found at the product website, www.acnemedrecall.com. No action is required of local health departments at this time for any of these recalls. If any requests for assistance are received from either the FDA or USDA, the Food and Drug Safety Program will contact you. For additional information regarding these recalls, please click on the weblink below.
Johnson & Johnson . Merck Consumer Pharmaceuticals Company (JJMCP) is voluntarily recalling approximately 12,000 units of Infants' MYLICON® GAS RELIEF
Johnson & Johnson . Merck Consumer Pharmaceuticals Company (JJMCP) is voluntarily recalling approximately 12,000 units of Infants' MYLICON® GAS RELIEF DYE FREE drops (simethicone-antigas) non-staining sold in 1 oz. plastic bottles that were distributed after October 5, 2008 nationwide. The company is taking this action in consultation with the U.S. Food and Drug Administration (FDA). Although the potential for serious medical events is low, the company is implementing this recall to the consumer level as a precaution after determining that some bottles could include metal fragments that were generated during the manufacturing process. If any medical events were to occur, most are expected to be temporary and resolve without medical treatment. Parents who have given the product to their infant and are concerned should contact their health care provider immediately.The two lots of Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining 1 oz. bottles included in the recall are:ProductCode # Lot # ExpProduct 71683791111-1SMF00709/10 Infants' Mylicon® Gas Relief Dye Free Non-Staining Drops 1 oz.71683791111-1SMF008 09/10 Infants' Mylicon® Gas Relief Dye Free Non-Staining Drops 1 oz.Consumers can find the lot numbers on the bottom of the box containing the product and also on the lower left side of the sticker on the product bottle.Consumers who purchased Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining included in this recall should immediately stop using the product and contact the company at 1-800-222-9435 (Monday - Friday, 8:00 a.m. - 8:00 p.m. EST) or via the internet at www.mylicon.com for instructions regarding how to dispose of the product and request a replacement or refund.Infants' MYLICON® drops are sold over-the counter, in retail stores and pharmacies, as an anti-gas medicine to relieve the discomfort of infant gas frequently caused by air swallowing or by certain formulas or foods. The recall does not affect any Original Infants' MYLICON® GAS RELIEF products (1/2 oz. or 1 oz. size) or Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining (1/2 oz. size). The manufacturer has instructed retailers and wholesalers to return their inventories.Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Amy's Kitchen Inc. of Santa Rosa, California is voluntarily recalling Tofu Scramble in a Pocket Sandwich Lot
. Amy's Kitchen Inc. of Santa Rosa, California is voluntarily recalling Tofu Scramble in a Pocket Sandwich Lot 10 H148, because of the presence of milk in a product that is labeled non-dairy. The 4.0 oz net wt frozen product, sold in U.S. grocery stores, comes in a retail package labeled as Amy's Tofu Scramble in a Pocket Sandwich. The code date printed in white on the easy open zipper end is 10 H148 A,B,C or DThe products could cause an allergic reaction if consumed by any individuals allergic to milk. People who have an allergy or severe sensitivity to dairy products run the risk of serious or life-threatening allergic reaction if they consume the product. Consumers without milk allergies can safely consume the product.The recall was initiated after one report of an allergic reaction due to this product, which was not labeled as containing dairy ingredients. Testing has shown the presence of milk. No other products or code dates of Amy's Kitchen products are affected by this recall. Consumers allergic to milk should contact Amy's Kitchen for a replacement or refund. The product is distributed to retailers only. Retailers are instructed to destroy the affected product. Amy's Kitchen is cooperating with FDA and will also issue an alert via the Food Allergy and Anaphylaxis Network.For instructions or questions, consumers may call the company collect: 707-568-4500 and ask for the consumer services department at ext 4571. Consumers who are not allergic to milk ingredients can consume the product or call for a full refund.
The following products are subject to recall:* 20-ounce, cartons of "#584 SCHWAN'S STUFFED CHICKEN KIEV."
The following products are subject to recall:* 20-ounce, cartons of "#584 SCHWAN'S STUFFED CHICKEN KIEV." Each carton contains 4 individually wrapped boneless breast units. Ink-jetted on the side of each carton is a product identification code of "T282171000," as well as a code of "21781" on each wrapper. Each carton bears the USDA mark of inspection. * 20-ounce, cartons of "#584 SCHWAN'S STUFFED CHICKEN KIEV." Each carton contains 4 individually wrapped boneless breast units. Ink-jetted on the side of each carton is a product identification code of "T281382000," as well as a code of "13882" on each wrapper. Each carton bears the USDA mark of inspection. * 20-ounce, cartons of "#584 SCHWAN'S STUFFED CHICKEN KIEV." Each carton contains 4 individually wrapped boneless breast units. Ink-jetted on the side of each carton is a product identification code of "T281541000," as well as a code of "15481" on each wrapper. Each carton bears the USDA mark of inspection. A sample photo is attached above for your reference.The products were produced on May 17, June 2 and August 4, and were made available for catalog or internet purchase from the Schwan's Home Service, Inc. by consumers nationwide. The problem was discovered after the Schwan's Home Service, Inc. received consumer complaints of finding pieces of rubber in the product. FSIS has not received any reports of injury at this time. Anyone concerned about an injury from consumption of the products should contact a physician. Media with questions about the recall should contact company Barber Foods Company Chief Financial Officer Vicki Mann at (207) 482-5503. Consumers with questions about the recall should contact Schwan's Home Service, Inc. at (888) 724-9267.
Monday, November 3, 2008
Progresso Hearty Tomato Soup Recall
Progresso Hearty Tomato Soup Recall
Case -UPC 41196910681
Case Date Code – 06sep0 nv
Can date code – 19may10 nv
As you may have heard, General Mills today announced a Class 1 Recall on its Progresso Hearty Tomato Soup. Our records indicate that General Mills did NOT ship this recalled product to any of your facilities. If you received this product from other sources, please contact your General Mills customer service representative immediately.
The recall was prompted by a mislabeling situation involving a limited number of cases produced on a portion of a single days’ production. In error, Progresso Hearty Tomato Soup labels were placed on a limited number of Progresso Light Vegetable and Noodle Soup cans. As a result, the correct allergens were not listed on the label, specifically egg, milk and soy.
Case -UPC 41196910681
Case Date Code – 06sep0 nv
Can date code – 19may10 nv
As you may have heard, General Mills today announced a Class 1 Recall on its Progresso Hearty Tomato Soup. Our records indicate that General Mills did NOT ship this recalled product to any of your facilities. If you received this product from other sources, please contact your General Mills customer service representative immediately.
The recall was prompted by a mislabeling situation involving a limited number of cases produced on a portion of a single days’ production. In error, Progresso Hearty Tomato Soup labels were placed on a limited number of Progresso Light Vegetable and Noodle Soup cans. As a result, the correct allergens were not listed on the label, specifically egg, milk and soy.
Mars Petcare US announced a voluntary recall of a limited number of bags of SPECIAL KITTY® Gourmet Blend dry cat food
Mars Petcare US announced a voluntary recall of a limited number of bags of SPECIAL KITTY® Gourmet Blend dry cat food sold at Wal-Mart locations in Connecticut, Delaware, Massachusetts, Maryland, Maine, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Virginia, Vermont, and West Virginia. The pet food is being voluntarily recalled following a positive test result indicating a potential contamination with Salmonella. This product should not be sold or fed to pets. Pet owners should dispose of product in a safe manner (example, a securely covered trash receptacle) and return the empty bag to the store where purchased for a full refund.Salmonella can cause serious infections in dogs and cats, and, if there is cross contamination caused by handling of the pet food, in people as well, especially children, the aged, and people with compromised immune systems. Healthy people potentially infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. On rare occasions, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Animals can be carriers with no visible symptoms and potentially infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.There have been no complaints or reports of illness resulting from consumption or handling of the recalled product.Pet owners who have questions about the recall should call 1-877-568-4463 or visit www.petcare.mars.com.Recalled Pet FoodProduct: SPECIAL KITTY® Gourmet Blend Dry Cat FoodBest If Used By Date: AUG 11 09Best If Used By Date Location: Back of bagProduction Lot Code: 50 XXXX X (Found on back of bag just after "Best If Used By" date. Consumers should look for "50" as the first two digits of the second line.)UPC Code: UPC code numbers can be found directly underneath the bar code on the package. Please find recalled pet food UPC information below.3.5 lb.SPECIAL KITTY® Gourmet Blend 81131 175467 lb.SPECIAL KITTY® Gourmet Blend 81131 1754718 lb.SPECIAL KITTY® Gourmet Blend 81131 17548Affected Stores: Wal-Mart locations in Connecticut, Delaware, Massachusetts, Maryland, Maine, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Virginia, Vermont, and West Virginia.In an effort to prevent the transmission of Salmonella from pets to family members and care givers, the FDA recommends that everyone follow appropriate pet food handling guidelines when feeding their pets. A list of safe pet food handling tips can be found at: www.fda.gov/consumer/updates/petfoodtips080307.htmlPet owners who have questions about the recall should call 1-877-568-4463 or visit www.petcare.mars.com. No action is required of local health departments at this time for this recall. If any requests for assistance are received from FDA, the Food and Drug Safety Program will contact you. For additional information regarding warnings and recalls, please click on the weblink below.
Friday, October 24, 2008
Harry and David, of Medford, Oregon, is voluntarily recalling approximately 400 1 lb. 4 oz. boxes labeled Harry & David Moose Munch Confection, Milk C
Harry and David, of Medford, Oregon, is voluntarily recalling approximately 400 1 lb. 4 oz. boxes labeled Harry & David Moose Munch Confection, Milk Chocolate Gingerbread because the package may contain a different Moose Munch product which contains pecans not declared on the ingredient statement. People who have an allergy or severe sensitivity to pecans run the risk of serious or life-threatening allergic reaction if they consume this product.Affected product was distributed throughout the United States under the Harry & David brand only in Harry and David stores. Harry and David is recalling 1 lb. 4 oz. boxes of Harry & David Moose Munch Confection, Milk Chocolate with a "Best if used by" date of 06/28/09. The "Best if used by" date is located on a sticker on the bottom of the box. The bottom of the box also has the stock identifying number RSD142014 printed on it. This lot of product was sold beginning 10/09/08. The popcorn-based confection is packaged in 1 lb. 4 oz. brown and white paperboard boxes. The boxes have a slight wedge shape and feature a large white moose image on the front. Inside the boxes are clear plastic bags of the confection.There have been no illnesses or injuries reported to date. Anyone concerned about an illness/injury should contact a physician immediately.This problem, which was discovered on October 21st, 2008, occurred because Dark Chocolate Butter Pecan Moose Munch® Confection was inadvertently packed in a Milk Chocolate Gingerbread outer box. It is estimated that fewer than 60 such boxes were produced.Consumers with product may return it to any Harry and David retail store for a full refund. Consumers with questions about the recalled product may phone the Harry and David Customer Service division at 800-233-1101, 24 hours a day. No action is required of local health departments at this time for this recall. If any requests for assistance are received from FDA, the Food and Drug Safety Program will contact you. For additional information regarding warnings and recalls, please click on the weblink below.
Monday, October 20, 2008
Recall of Koala's March Crème filled Cookies Due to Melamine Contamination
NJLINCS Health Alert Network
Public Health Info
Distributed by the New Jersey Department of Health and Senior Services
Subject: Recall of Koala's March Crème filled Cookies Due to Melamine Contamination
Date: 10/20/2008; 11:18:02
Message#: 100966-10-20-2008-PHIN
Contact Info: Alan L. Talarsky, NJDHSS/CEHS/Food and Drug Safety ProgramPhone: 609-588-3123; Email: at2@njlincs.net
Attachments: Lotte_Koala's_March_Cookies.jpg
Please review the following message from Alan Talarsky, Environmental Scientist 1, Food and Drug Safety Program, DHSS regarding the U.S. Food and Drug Administration's Class 1 recall of Lotte USA's Koala's March Crème-filled Cookies due to melamine contamination.Lotte USA, Inc., Battle Creek, MI initiated a recall of all Koalas' March Cookies on September 29, 2008 because they were produced in China and they may be contaminated with melamine. The products are packaged in a plastic overwrap and the recall includes the following products:Koala March King Size Chocolate 1.8 oz 50 gramsUPC 0 81900 00001 7Koala March King Size Strawberry 1.8 oz/50 gramsUPC 0 81900 00007 9Koala March King Size White Chocolate 1.8 oz/50 gramsUPC 0 81900 00011 6Koala March Family Pack Chocolate 9.5 oz/270 gramsUPC 0 81900 08001 9Koala March Family Pack Strawberry 9.5 oz/270 gramsUPC 0 81900 08002 6Koala March Family Pack White Chocolate 9.5 oz/270 gramsUPC 0 81900 08011 8Koala March Family Pack Chestnut 9.5 oz/270 gramsUPC 0 81900 08010 1Koala March Family Hawaii Chocolate 9.5 oz/270 gramsUPC 0 81900 08003 3Koala March Family Hawaii Pineapple 9.5 oz/270 gramsUPC 0 81900 08004 0A sample photo of these products is attached above for your reference.The product were distributed nationwide and to Canada through wholesale distributors and retail stores. Lotte USA, Inc. is not aware of any illnesses or injuries associated with these products.Individuals who have experienced any health problems after consuming the Koala March cookies are advised to contact their health care professional.Customers who have purchased Koala's March cookies are urged to return them to the place of purchase for a full refund or discard it in their trash. Consumers with questions may contact the company at (269) 963-6664, Monday to Friday, 9:00 to 5:00 Eastern Standard Time. No action is required of local health departments at this time for this recall. However, inspectors should take appropriate enforcement action if these products are encountered during routine inspections.
Public Health Info
Distributed by the New Jersey Department of Health and Senior Services
Subject: Recall of Koala's March Crème filled Cookies Due to Melamine Contamination
Date: 10/20/2008; 11:18:02
Message#: 100966-10-20-2008-PHIN
Contact Info: Alan L. Talarsky, NJDHSS/CEHS/Food and Drug Safety ProgramPhone: 609-588-3123; Email: at2@njlincs.net
Attachments: Lotte_Koala's_March_Cookies.jpg
Please review the following message from Alan Talarsky, Environmental Scientist 1, Food and Drug Safety Program, DHSS regarding the U.S. Food and Drug Administration's Class 1 recall of Lotte USA's Koala's March Crème-filled Cookies due to melamine contamination.Lotte USA, Inc., Battle Creek, MI initiated a recall of all Koalas' March Cookies on September 29, 2008 because they were produced in China and they may be contaminated with melamine. The products are packaged in a plastic overwrap and the recall includes the following products:Koala March King Size Chocolate 1.8 oz 50 gramsUPC 0 81900 00001 7Koala March King Size Strawberry 1.8 oz/50 gramsUPC 0 81900 00007 9Koala March King Size White Chocolate 1.8 oz/50 gramsUPC 0 81900 00011 6Koala March Family Pack Chocolate 9.5 oz/270 gramsUPC 0 81900 08001 9Koala March Family Pack Strawberry 9.5 oz/270 gramsUPC 0 81900 08002 6Koala March Family Pack White Chocolate 9.5 oz/270 gramsUPC 0 81900 08011 8Koala March Family Pack Chestnut 9.5 oz/270 gramsUPC 0 81900 08010 1Koala March Family Hawaii Chocolate 9.5 oz/270 gramsUPC 0 81900 08003 3Koala March Family Hawaii Pineapple 9.5 oz/270 gramsUPC 0 81900 08004 0A sample photo of these products is attached above for your reference.The product were distributed nationwide and to Canada through wholesale distributors and retail stores. Lotte USA, Inc. is not aware of any illnesses or injuries associated with these products.Individuals who have experienced any health problems after consuming the Koala March cookies are advised to contact their health care professional.Customers who have purchased Koala's March cookies are urged to return them to the place of purchase for a full refund or discard it in their trash. Consumers with questions may contact the company at (269) 963-6664, Monday to Friday, 9:00 to 5:00 Eastern Standard Time. No action is required of local health departments at this time for this recall. However, inspectors should take appropriate enforcement action if these products are encountered during routine inspections.
Wednesday, October 15, 2008
Class 1 recall of YILI Brand Sour Milk Drink and YILI Brand Pure Milk Drink due to melamine contamination
Please review the following message from Alan Talarsky, Environmental Scientist 1, Food and Drug Safety Program, DHSS regarding the U.S. Food and Drug Administration's Class 1 recall of YILI Brand Sour Milk Drink and YILI Brand Pure Milk Drink due to melamine contamination.HUA XIA Food Trade USA, Inc. of Flushing, NY, is recalling YILI Brand Sour Milk Drink packaged in 250ml flexible paperboard boxes (all codes and all lots are affected) and YILI Brand Pure Milk Drink packaged in 250ml flexible paperboard boxes (all codes and all lots are affected) because it may be contaminated with melamine.Consumers who have the product which is being recalled should stop using it immediately. If consumers have questions about possible health risks, they should contact their doctor.YILI Brand Sour Milk Drink and YILI Brand Pure Milk Drink were distributed to New York City through Asian retail grocery stores. The Food and Drug Safety Program is not aware of this product being distributed in New Jersey, but is sending you this message out of an abundance of caution.The products being recalled are:* YILI Brand Sour Milk Drink is packaged in 250ml flexible paperboard boxes with blue, red and green Chinese writing. There is a picture of an Asian man in a green shirt and white tie clapping his hands on the face of the box. All codes and all lots are affected. * YILI Brand Pure Milk Drink packaged in 250ml flexible paperboard boxes with black, red and white writing, the writing on the package is in both English and Chinese. There is a picture of two cows playing basketball on the face of the box. All codes and all lots are affected. No illnesses have been reported to date.The recall was initiated after FDA testing discovered that the product was found to contain Melamine. Consumers who have purchased YILI Brand Sour Milk or YILI Brand Pure Milk Drink are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at (917) 216-0575, Monday to Friday, 9:00 to 5:00, Eastern Standard Time.No action is required of local health departments at this time for this recall. However, inspectors should take appropriate enforcement action if these products are encountered during routine inspections.If any requests for assistance are received from FDA, the Food and Drug Safety Program will contact you. For additional information regarding warnings and recalls, please click on the weblink below.**********************************************************************************
Wednesday, October 8, 2008
Undeclared Sulfites in “Shad Raisins
CONTACT: FOR RELEASE:
Jessica Chittenden Immediately, Monday
518-457-3136 October 6, 2008
***CONSUMER ALERT***
Undeclared Sulfites in “Shad Raisins”
New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Fatima Brothers Inc. of 54-08 43rd St Maspeth, New York 11378 is recalling "Shad Raisins" due to the presence of undeclared sulfites. People who have severe sensitivity to sulfites may run the risk of serious or life-threatening reactions if they consume this product.
The recalled "Shad Raisins" were packaged in uncoded, 7-ounce plastic bags. “Shad Raisins” were distributed in New York City.
Routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the product contained high levels of sulfites which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date to this Department in connection with this product. Consumers who have purchased "Shad Raisins" should return them to the place of purchase.
Jessica Chittenden Immediately, Monday
518-457-3136 October 6, 2008
***CONSUMER ALERT***
Undeclared Sulfites in “Shad Raisins”
New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Fatima Brothers Inc. of 54-08 43rd St Maspeth, New York 11378 is recalling "Shad Raisins" due to the presence of undeclared sulfites. People who have severe sensitivity to sulfites may run the risk of serious or life-threatening reactions if they consume this product.
The recalled "Shad Raisins" were packaged in uncoded, 7-ounce plastic bags. “Shad Raisins” were distributed in New York City.
Routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the product contained high levels of sulfites which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date to this Department in connection with this product. Consumers who have purchased "Shad Raisins" should return them to the place of purchase.
Possible Botulism Contamination in “Frozen Salted Croaker
CONTACT: FOR RELEASE:
Jessica Chittenden Immediately, Monday
518-457-3136 October 6, 2008
***CONSUMER ALERT***
Possible Botulism Contamination in “Frozen Salted Croaker”
New York State Agriculture Commissioner Patrick Hooker today alerted consumers not to eat “Frozen Salted Croaker” distributed by YS Trading Corp of 38-21 23rd Street, Long Island City, New York 11101 because the product was uneviscerated.
The “Frozen Salted Croaker” was sold in Hicksville, New York, Flushing, New York, and New Jersey in un-coded, unlabeled plastic bags.
Uneviscerated fish is prohibited under New York State Department of Agriculture and Markets’ regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of Botulism poisoning.
Because the fish is uneviscerated, the product may become contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food-borne illness. Symptoms of Botulism include blurred or double vision, general weakness, poor reflexes, difficulty swallowing and respiratory paralysis.
The "Frozen Salted Croaker" was found by a New York State Department of Agriculture and Markets food inspector during a routine inspection. Subsequent analysis by New York State Food Laboratory personnel confirmed the product to be uneviscerated.
No illnesses have been reported to date in connection with the product. Consumers who have this product are advised not to eat it.
Jessica Chittenden Immediately, Monday
518-457-3136 October 6, 2008
***CONSUMER ALERT***
Possible Botulism Contamination in “Frozen Salted Croaker”
New York State Agriculture Commissioner Patrick Hooker today alerted consumers not to eat “Frozen Salted Croaker” distributed by YS Trading Corp of 38-21 23rd Street, Long Island City, New York 11101 because the product was uneviscerated.
The “Frozen Salted Croaker” was sold in Hicksville, New York, Flushing, New York, and New Jersey in un-coded, unlabeled plastic bags.
Uneviscerated fish is prohibited under New York State Department of Agriculture and Markets’ regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of Botulism poisoning.
Because the fish is uneviscerated, the product may become contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food-borne illness. Symptoms of Botulism include blurred or double vision, general weakness, poor reflexes, difficulty swallowing and respiratory paralysis.
The "Frozen Salted Croaker" was found by a New York State Department of Agriculture and Markets food inspector during a routine inspection. Subsequent analysis by New York State Food Laboratory personnel confirmed the product to be uneviscerated.
No illnesses have been reported to date in connection with the product. Consumers who have this product are advised not to eat it.
Monday, October 6, 2008
McCormick's Enchilada Sauce Mix, because it contains undeclared milk ingredients
Please review the following message from Alan Talarsky, Environmental Scientist 1, Food and Drug Safety Program, DHSS regarding the U.S. Food and Drug Administration's Class 1 recall of McCormick's Enchilada Sauce Mix, because it contains undeclared milk ingredients, an allergen.McCormick & Company, Incorporated has announced a voluntary recall of McCormick Enchilada Sauce Mix with UPC Code 52100091600 sold under the McCormick brand. The McCormick Enchilada Sauce Mix contains undeclared milk ingredients. People who have allergies to milk run the risk of serious or life threatening allergic reactions if they consume this product.The McCormick Enchilada Sauce Mix was distributed to grocery stores nationally beginning on September 17, 2008. The product comes in 1.5 oz. pouches with an expiration date of "best by" AUG2910CH. The date is found printed in black on the back, bottom left of the pouch. A photo of this product is attached above for your reference.The recall was initiated after it was discovered that product containing the milk ingredient was distributed in packaging that did not reveal the presence of milk as an ingredient. No illnesses or allergic reactions have been reported to date. No other McCormick products are involved in this recall.All grocery outlets that sell McCormick Enchilada Sauce Mix (UPC Code 52100091600 with expiration date "best by" AUG2910CH) have been notified to remove the product from their shelves immediately, and consumers who have purchased this product should return it to the place of purchase for a full refund. Consumers with questions may contact McCormick at 1-800-632-5847.No action is required of local health departments at this time for this recall. If any requests for assistance are received from FDA, the Food and Drug Safety Program will contact you. For additional information regarding warnings and recalls, please click on the weblink below.
Undeclared Sulfites in “Shad Raisins” and Possible Botulism Contamination in “Frozen Salted Croaker.”
Please see the attached two consumer alerts from the NYS Department of Agriculture & Markets for Undeclared Sulfites in “Shad Raisins” and Possible Botulism Contamination in “Frozen Salted Croaker.”
CONTACT: FOR RELEASE:
Jessica Chittenden Immediately, Monday
518-457-3136 October 6, 2008
***CONSUMER ALERT***
Undeclared Sulfites in “Shad Raisins”
New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Fatima Brothers Inc. of 54-08 43rd St Maspeth, New York 11378 is recalling "Shad Raisins" due to the presence of undeclared sulfites. People who have severe sensitivity to sulfites may run the risk of serious or life-threatening reactions if they consume this product.
The recalled "Shad Raisins" were packaged in uncoded, 7-ounce plastic bags. “Shad Raisins” were distributed in New York City.
Routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the product contained high levels of sulfites which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date to this Department in connection with this product. Consumers who have purchased "Shad Raisins" should return them to the place of purchase.
###
CONTACT: FOR RELEASE:
Jessica Chittenden Immediately, Monday
518-457-3136 October 6, 2008
***CONSUMER ALERT***
Possible Botulism Contamination in “Frozen Salted Croaker”
New York State Agriculture Commissioner Patrick Hooker today alerted consumers not to eat “Frozen Salted Croaker” distributed by YS Trading Corp of 38-21 23rd Street, Long Island City, New York 11101 because the product was uneviscerated.
The “Frozen Salted Croaker” was sold in Hicksville, New York, Flushing, New York, and New Jersey in un-coded, unlabeled plastic bags.
Uneviscerated fish is prohibited under New York State Department of Agriculture and Markets’ regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of Botulism poisoning.
Because the fish is uneviscerated, the product may become contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food-borne illness. Symptoms of Botulism include blurred or double vision, general weakness, poor reflexes, difficulty swallowing and respiratory paralysis.
The "Frozen Salted Croaker" was found by a New York State Department of Agriculture and Markets food inspector during a routine inspection. Subsequent analysis by New York State Food Laboratory personnel confirmed the product to be uneviscerated.
No illnesses have been reported to date in connection with the product. Consumers who have this product are advised not to eat it.
CONTACT: FOR RELEASE:
Jessica Chittenden Immediately, Monday
518-457-3136 October 6, 2008
***CONSUMER ALERT***
Undeclared Sulfites in “Shad Raisins”
New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Fatima Brothers Inc. of 54-08 43rd St Maspeth, New York 11378 is recalling "Shad Raisins" due to the presence of undeclared sulfites. People who have severe sensitivity to sulfites may run the risk of serious or life-threatening reactions if they consume this product.
The recalled "Shad Raisins" were packaged in uncoded, 7-ounce plastic bags. “Shad Raisins” were distributed in New York City.
Routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the product contained high levels of sulfites which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date to this Department in connection with this product. Consumers who have purchased "Shad Raisins" should return them to the place of purchase.
###
CONTACT: FOR RELEASE:
Jessica Chittenden Immediately, Monday
518-457-3136 October 6, 2008
***CONSUMER ALERT***
Possible Botulism Contamination in “Frozen Salted Croaker”
New York State Agriculture Commissioner Patrick Hooker today alerted consumers not to eat “Frozen Salted Croaker” distributed by YS Trading Corp of 38-21 23rd Street, Long Island City, New York 11101 because the product was uneviscerated.
The “Frozen Salted Croaker” was sold in Hicksville, New York, Flushing, New York, and New Jersey in un-coded, unlabeled plastic bags.
Uneviscerated fish is prohibited under New York State Department of Agriculture and Markets’ regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of Botulism poisoning.
Because the fish is uneviscerated, the product may become contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food-borne illness. Symptoms of Botulism include blurred or double vision, general weakness, poor reflexes, difficulty swallowing and respiratory paralysis.
The "Frozen Salted Croaker" was found by a New York State Department of Agriculture and Markets food inspector during a routine inspection. Subsequent analysis by New York State Food Laboratory personnel confirmed the product to be uneviscerated.
No illnesses have been reported to date in connection with the product. Consumers who have this product are advised not to eat it.
Monday, September 29, 2008
LION PAVILION ISSUES ALERT ON UNDECLARED SULFITES IN YULANPIAN BRAND DRIED SLICES OF TENDER BAMBOO SHOOTS
Lion Pavilion LTD
541 Gardner Ave Brooklyn NY 11222 Tel: 718-384-6951 FAX: 718-384-6953
PRESS RELEASE
FOR IMMEDIATE RELEASE September 26, 2008
Jeannette Chen / 718-384-6951
LION PAVILION ISSUES ALERT ON UNDECLARED SULFITES IN YULANPIAN BRAND DRIED SLICES OF TENDER BAMBOO SHOOTS
LION PAVILION LTD. of 541 Gardner Avenue, Brooklyn, NY 11222 is recalling Yulanpian Brand Dried Slices of Tender Bamboo Shoots because it contains undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
Yulanpian Brand Dried Slices of Tender Bamboo Shoots is sold in a 230gram, clear plastic package with the following code: 2008.1.3 and was distributed nationwide. It is a product of China.
The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in Yulanpian Brand Dried Slices of Tender Bamboo Shoots which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses or allergic reactions involving this product have been reported to date. Consumers who have purchased Yulanpian Brand Dried Slices of Tender Bamboo Shoots are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 718-384-6951.
541 Gardner Ave Brooklyn NY 11222 Tel: 718-384-6951 FAX: 718-384-6953
PRESS RELEASE
FOR IMMEDIATE RELEASE September 26, 2008
Jeannette Chen / 718-384-6951
LION PAVILION ISSUES ALERT ON UNDECLARED SULFITES IN YULANPIAN BRAND DRIED SLICES OF TENDER BAMBOO SHOOTS
LION PAVILION LTD. of 541 Gardner Avenue, Brooklyn, NY 11222 is recalling Yulanpian Brand Dried Slices of Tender Bamboo Shoots because it contains undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
Yulanpian Brand Dried Slices of Tender Bamboo Shoots is sold in a 230gram, clear plastic package with the following code: 2008.1.3 and was distributed nationwide. It is a product of China.
The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in Yulanpian Brand Dried Slices of Tender Bamboo Shoots which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses or allergic reactions involving this product have been reported to date. Consumers who have purchased Yulanpian Brand Dried Slices of Tender Bamboo Shoots are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 718-384-6951.
The U.S. Food and Drug Administration (FDA) is alerting consumers that seven Mr. Brown instant coffee and milk tea products are being recalled
The U.S. Food and Drug Administration (FDA) is alerting consumers that seven Mr. Brown instant coffee and milk tea products are being recalled by the Taiwanese company, King Car Food Industrial Co. Ltd., due to possible contamination with melamine. The recalled products are:
Mr. Brown Mandheling Blend Instant Coffee (3-in-1)
Mr. Brown Arabica Instant Coffee (3-in-1)
Mr. Brown Blue Mountain Blend Instant Coffee (3-in-1)
Mr. Brown Caramel Macchiato Instant Coffee (3-in-1)
Mr. Brown French Vanilla Instant Coffee (3-in-1)
Mr. Brown Mandhling Blend instant Coffee (2-in-1)
Mr. Brown Milk Tea (3-in-1)
The FDA recommends that consumers not consume any of the above Mr. Brown instant coffee and milk tea products. The FDA also recommends that retailers and foodservice operators remove the products from sale or service.
As of September 25, 2008, the FDA testing of milk based products imported into the United States from China has not found melamine contamination.
The FDA is working with regulatory agencies in other countries. The New Zealand Food Safety Authority reports that its testing of White Rabbit Creamy Candies has shown melamine contamination at high levels. In light of the widespread contamination of milk and milk-based products in China and the New Zealand Food Safety Authority’s finding, the FDA recommends that consumers not eat White Rabbit Creamy Candy and that retailers and foodservice operations remove the product from sale or service.To date, the FDA is not aware of any illnesses in the United States stemming from consumption of either White Rabbit Creamy Candy or the Mr. Brown instant coffee and milk tea products.
Individuals who have experienced any health problems after consuming either White Rabbit Creamy Candy or any of the identified Mr. Brown coffee and tea products are advised to contact their health care professional.
Background
On September 12, 2008, in light of reports from China of melamine contaminated infant formula, the FDA issued a Health Information Advisory to assure the American public that there is no known threat of contamination in infant formula manufactured by companies that have met the requirements to sell such products in the United States. That advisory also warned members of Chinese communities in the United States that infant formula manufactured in China, possibly available for purchase at Asian markets, could pose a risk to infants.
The FDA had contacted the companies who manufacture infant formula for distribution in the United States and received, from the companies, information that they are not importing formula or sourcing milk-based materials from China.
At the same time, the FDA—in conjunction with state and local officials—began a nation-wide investigation to check Asian markets for Chinese manufactured infant formula that may have been brought into the United States. In particular, this effort focused on areas of the country with large Chinese communities, such as Los Angeles, San Francisco, Seattle and New York. To date, investigators have visited more than 1,400 retail markets and have not found Chinese infant formula present on shelves in these markets.
The FDA also advises consumers not to purchase infant formula manufactured in China from Internet sites or from other sources.
The FDA has taken, and will continue to take, proactive measures to help ensure the safety of the American food supply. In conjunction with state and local officials, the FDA will continue to check Asian markets for food items that are imported from China and that could contain a significant amount of milk or milk proteins. In addition, the FDA has broadened its domestic and import sampling and testing of milk-derived ingredients and finished food products containing milk, such as candies, desserts, and beverages that could contain these ingredients from Chinese sources. Milk-derived ingredients include whole milk powder, non-fat milk powder, whey powder, lactose powder, and casein.
In addition to state and local governments, the FDA is working in close cooperation with Customs and Border Protection within the U.S. Department of Homeland Security, the U.S. Department of Agriculture, other federal agencies, and foreign governments.
Mr. Brown Mandheling Blend Instant Coffee (3-in-1)
Mr. Brown Arabica Instant Coffee (3-in-1)
Mr. Brown Blue Mountain Blend Instant Coffee (3-in-1)
Mr. Brown Caramel Macchiato Instant Coffee (3-in-1)
Mr. Brown French Vanilla Instant Coffee (3-in-1)
Mr. Brown Mandhling Blend instant Coffee (2-in-1)
Mr. Brown Milk Tea (3-in-1)
The FDA recommends that consumers not consume any of the above Mr. Brown instant coffee and milk tea products. The FDA also recommends that retailers and foodservice operators remove the products from sale or service.
As of September 25, 2008, the FDA testing of milk based products imported into the United States from China has not found melamine contamination.
The FDA is working with regulatory agencies in other countries. The New Zealand Food Safety Authority reports that its testing of White Rabbit Creamy Candies has shown melamine contamination at high levels. In light of the widespread contamination of milk and milk-based products in China and the New Zealand Food Safety Authority’s finding, the FDA recommends that consumers not eat White Rabbit Creamy Candy and that retailers and foodservice operations remove the product from sale or service.To date, the FDA is not aware of any illnesses in the United States stemming from consumption of either White Rabbit Creamy Candy or the Mr. Brown instant coffee and milk tea products.
Individuals who have experienced any health problems after consuming either White Rabbit Creamy Candy or any of the identified Mr. Brown coffee and tea products are advised to contact their health care professional.
Background
On September 12, 2008, in light of reports from China of melamine contaminated infant formula, the FDA issued a Health Information Advisory to assure the American public that there is no known threat of contamination in infant formula manufactured by companies that have met the requirements to sell such products in the United States. That advisory also warned members of Chinese communities in the United States that infant formula manufactured in China, possibly available for purchase at Asian markets, could pose a risk to infants.
The FDA had contacted the companies who manufacture infant formula for distribution in the United States and received, from the companies, information that they are not importing formula or sourcing milk-based materials from China.
At the same time, the FDA—in conjunction with state and local officials—began a nation-wide investigation to check Asian markets for Chinese manufactured infant formula that may have been brought into the United States. In particular, this effort focused on areas of the country with large Chinese communities, such as Los Angeles, San Francisco, Seattle and New York. To date, investigators have visited more than 1,400 retail markets and have not found Chinese infant formula present on shelves in these markets.
The FDA also advises consumers not to purchase infant formula manufactured in China from Internet sites or from other sources.
The FDA has taken, and will continue to take, proactive measures to help ensure the safety of the American food supply. In conjunction with state and local officials, the FDA will continue to check Asian markets for food items that are imported from China and that could contain a significant amount of milk or milk proteins. In addition, the FDA has broadened its domestic and import sampling and testing of milk-derived ingredients and finished food products containing milk, such as candies, desserts, and beverages that could contain these ingredients from Chinese sources. Milk-derived ingredients include whole milk powder, non-fat milk powder, whey powder, lactose powder, and casein.
In addition to state and local governments, the FDA is working in close cooperation with Customs and Border Protection within the U.S. Department of Homeland Security, the U.S. Department of Agriculture, other federal agencies, and foreign governments.
Wednesday, September 24, 2008
Recalls of Mut Gung brand Sweetened Ginger and Ying Feng brand Pumpkin Seeds, both due to undeclared sulfites, an allergen.1.
Please review the following messages from Alan Talarsky, Environmental Scientist 1, Food and Drug Safety Program, DHSS regarding the U.S. Food and Drug Administration's Class 1 Recalls of Mut Gung brand Sweetened Ginger and Ying Feng brand Pumpkin Seeds, both due to undeclared sulfites, an allergen.1. K-FAT INC. of 13 Meadow St., Brooklyn, NY 11206, is recalling its 150g packages of MUT GUNG SWEETENED GINGER because they contain undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious life-threatening allergic reactions if they consume this product.The product comes in a 150g clear plastic container. The recalled Mut Gung Sweetened Ginger was distributed nationwide in retail stores and through mail orders.The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in the 150g packages of Mut Gung Sweetened Ginger which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon digesting 10 milligrams or more of sulfites. Analysis of the Mut Gung Sweetened Ginger revealed they contained 94.5 mg per serving.No illnesses or allergic reactions involving this product have been reported to date. Consumers who have purchased 150g packages of Mut Gung Sweetened Ginger are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (718) 381-0306.**********************************************************************************2. Fine Land Corp of 239 Bay 20th Street, Brooklyn, NY 11214, is recalling Ying Feng Foodstuffs Brand Pumpkin Seeds because it contains undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.Ying Feng Foodstuffs Brand Pumpkin Seeds is sold in a 10 ounce, clear plastic package with the following code: EXP 03 25 2010 and was distributed nationwide. It is a product of China.The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in Ying Feng Foodstuffs Brand Pumpkin Seeds which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites. No illnesses or allergic reactions involving this product has been reported to date. Consumers who have purchased Ying Feng Foodstuffs Brand Pumpkin Seeds are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 718-714-1850. No action is required of local health departments at this time for any of these recalls. If any requests for assistance are received from the FDA or USDA, the Food and Drug Safety Program will contact you. For additional information regarding these recalls, please click on the weblink below.**********************************************************************************For all FDA-issued food recalls - http://www.fda.gov/opacom/7alerts.html
This information has been distributed to: DHSS Senior Staff; DHSS Staff; LINCS Coordinator Backups; LINCS Coordinators; LINCS Epidemiologists; LINCS Health Educators; LINCS Health Officer Assistants; LINCS Health Officers; LINCS Health Planners; LINCS IT Specialists; LINCS Partnership Coordinators; LINCS Public Health Nurses; LINCS Regional Health Planners; LINCS Team Members; LOCAL Health Officers; LOCAL Public Health; Food Safety Organizations
Further distribution of this message should be directed to: n/a
IMPORTANT NOTE: Please do not use reply feature of your email system. If you have questions about the content of this email or any of its attachments, please call your County/City LINCS agency for assistance. LINCS agencies are instructed to contact the individual listed in message above or on the attachment for questions concerning content.
This information has been distributed to: DHSS Senior Staff; DHSS Staff; LINCS Coordinator Backups; LINCS Coordinators; LINCS Epidemiologists; LINCS Health Educators; LINCS Health Officer Assistants; LINCS Health Officers; LINCS Health Planners; LINCS IT Specialists; LINCS Partnership Coordinators; LINCS Public Health Nurses; LINCS Regional Health Planners; LINCS Team Members; LOCAL Health Officers; LOCAL Public Health; Food Safety Organizations
Further distribution of this message should be directed to: n/a
IMPORTANT NOTE: Please do not use reply feature of your email system. If you have questions about the content of this email or any of its attachments, please call your County/City LINCS agency for assistance. LINCS agencies are instructed to contact the individual listed in message above or on the attachment for questions concerning content.
Monday, September 22, 2008
FDA Updates Health Information Advisory on Melamine Contamination
FDA Home Page Search FDA Site FDA A-Z Index Contact FDA
FDA Statement
FOR IMMEDIATE RELEASEStatementSeptember 20, 2008
Media Inquiries: Stephanie Kwisnek, 301-827-0955Consumer Inquiries: 888-INFO-FDA
FDA Updates Health Information Advisory on Melamine Contamination
On September 12, 2008, in light of reports from China of melamine contaminated infant formula, the FDA issued a Health Information Advisory to proactively reassure the American public that there is no known threat of contamination in infant formula manufactured by companies that have met the requirements to sell such products in the United States. That advisory also warned members of Chinese communities in the United States that infant formula manufactured in China, possibly available for purchase at Asian markets, could pose a risk to infants.
The FDA had contacted the companies who manufacture infant formula for distribution in the United States and received information from the companies that they are not importing formula or source materials from China.
At the same time, the FDA—in conjunction with state and local officials—began a nation-wide investigation to check Asian markets for Chinese manufactured infant formula that may have been brought into the United States. In particular, this effort focused on areas of the country with large Chinese communities, such as Los Angeles, San Francisco, Seattle and New York. To date, investigators have visited more than 1,000 retail markets and have not found Chinese infant formula present on shelves in these markets.
In addition, the FDA is advising consumers not to purchase infant formula manufactured in China from internet sites or from other sources.
FDA has taken, and will continue to take, proactive measures to help ensure the safety of the American food supply. In conjunction with state and local officials, FDA will continue to check retail stores for food items imported from China that could contain a significant amount of milk or milk proteins. Additionally, FDA is sampling and testing milk and milk-derived ingredients and finished food products that could contain these ingredients from Chinese sources. Milk-derived ingredients include whole milk powder, non-fat milk powder, whey powder, lactose powder, and casein. This sampling and testing is done when these ingredients or products are imported into the United States or found during visits to Asian markets. If the products are adulterated because they contain melamine and/or a melamine analog, FDA will take action to prevent the products from entering the U.S. food supply.
In addition to state and local governments, FDA is working in close cooperation with Customs and Border Protection within the U.S. Department of Homeland Security, the U.S. Department of Agriculture, other federal agencies, and foreign governments.
Thursday, September 18, 2008
Undeclared Sulfites in KFI Brand “Sweetened Ginger – Mut Gung
Undeclared Sulfites in KFI Brand “Sweetened Ginger – Mut Gung”
New York State Agriculture Commissioner Patrick Hooker today alerted consumers that K-Fat Incorporated located at 13 Meadow Street, Brooklyn, New York 11206 is recalling KFI brand “Sweetened Ginger – Mut Gung” due to the presence of undeclared sulfites. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product
The KFI brand “Sweetened Ginger – Mut Gung” is packaged in 150 gram un-coded, unlabeled plastic containers with plastic lids. This product was distributed nationwide. According to the label, the product is made in Vietnam.
Routine sampling by a New York State Department of Agriculture and Markets’ food inspector and subsequent analysis by New York State Food Laboratory personnel confirmed the product contained sulfites which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date to this Department in connection with this product. Sulfite sensitive consumers who have purchased KFI brand “Sweetened Ginger – Mut Gung” should return it to place of purchase.
New York State Agriculture Commissioner Patrick Hooker today alerted consumers that K-Fat Incorporated located at 13 Meadow Street, Brooklyn, New York 11206 is recalling KFI brand “Sweetened Ginger – Mut Gung” due to the presence of undeclared sulfites. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product
The KFI brand “Sweetened Ginger – Mut Gung” is packaged in 150 gram un-coded, unlabeled plastic containers with plastic lids. This product was distributed nationwide. According to the label, the product is made in Vietnam.
Routine sampling by a New York State Department of Agriculture and Markets’ food inspector and subsequent analysis by New York State Food Laboratory personnel confirmed the product contained sulfites which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date to this Department in connection with this product. Sulfite sensitive consumers who have purchased KFI brand “Sweetened Ginger – Mut Gung” should return it to place of purchase.
Monday, September 15, 2008
Mars Petcare US Issues Voluntary Recall of Everson, PA Plant Dry Pet Food Product due to Potential Salmonella Contamination
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Mars Petcare US Issues Voluntary Recall of Everson, PA Plant Dry Pet Food Product due to Potential Salmonella Contamination
Contact:Debra Fair(973) 691-3536
FOR IMMEDIATE RELEASE -- Fanklin, Tennessee -- September 12, 2008 -- Today, Mars Petcare US announced a voluntary recall of products manufactured at its Everson, Pennsylvania facility. The pet food is being voluntarily recalled because of potential contamination with Salmonella serotypeSchwarzengrund. This voluntary recall only affects the United States.
Salmonella can cause serious infections in dogs and cats, and, if there is cross contamination caused by handling of the pet food, in people as well, especially children, the aged, and people with compromised immune systems. Healthy people potentially infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. On rare occasions, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.
Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Animals can be carriers with no visible symptoms and can potentially infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.
The company stopped production at the Everson facility on July 29, 2008 when it was alerted of a possible link between dry pet food produced at the plant and two isolated cases of people infected with Salmonella Schwarzengrund.
Even though no direct link between product produced at Everson and human or pet illness has been made, Mars Petcare US is taking precautionary action to protect pets and their owners by announcing a voluntary recall of all products produced at the Everson facility beginning February 18, 2008 until July 29, 2008 when we stopped production.
The company is continuing to work collaboratively with the FDA to determine the nature and source of Salmonella Schwarzengrund at the Everson facility. Since it has not yet identified the source of the Salmonella Schwarzengrund at the Everson facility, Mars Petcare US does not plan to resume production out of a commitment to the safety of our pet owners and their pets, customers, and associates.
The top priority of Mars Petcare US has always been and continues to be the health and welfare of pets and their owners. Consumers can continue to have confidence in the quality and safety of the products produced at other Mars Petcare US facilities. Only those products which were produced at the Everson facility are impacted by the voluntary recall.
Many of the brands involved in the recall are national brands produced at multiple facilities. A chart for all products is below. For example, PEDIGREE® is manufactured in numerous facilities throughout the country, and Everson represents a very small portion of the manufacturing base – 2.7 percent of total PEDIGREE® production.
Mars Petcare US will work with retail customers to ensure that the recalled products are not on store shelves. These products should not be sold or fed to pets. In the event that consumers believe they have purchased products affected by this voluntary recall, they should return the product to the store where they purchased it for a full refund. Specific product details and other information can be found at www.petcare.mars.com
Please find recalled pet food UPC information below.
The products listed below are made at our Everson facility on behalf of a variety of retailers. All code dates, with the exception of PEDIGREE®, are listed in a similar format as noted below:Consumers should look for “17” as the first two digits of the second line. Sample:Best By Feb 18 0917 1445 1
For PEDIGREE® the Everson code date format is as follows:
Consumers should look for “PAE” on the bottom line – the sixth, seventh and eighth digits. Sample:PEDIGREE ® Small Crunchy BitesBest Before 02/2009808G1PAE01 12:00
In an effort to prevent the transmission of Salmonella from pets to family members and care givers, the FDA recommends that everyone follow appropriate pet food handling guidelines when feeding their pets. A list of safe pet food handling tips can be found at: www.fda.gov/consumer/updates/petfoodtips080307.html
Pet owners who have questions about the recall should call 1-877-568-4463 or visit www.petcare.mars.com.
Recalled Pet Food Note: If you see a product you purchased listed below, please review the code date information samples from above to confirm that your product is included in the recall.
Product Name / Bag Size
UPC
Product Name / Bag Size
UPC
Country Acres Cat Food 40#
16603 02181
Retriever Bites & Bones Dog Food 8#
79818 96757
Country Acres Ration Dog Food 40#
16603 02333
Retriever Bites & Bones Dog Food 20#
79818 96634
Country Acres 18% Dog Food 40#
16603 02331
Retriever Bites & Bones Dog Food 50#
49394 05666
Country Acres Hi Pro Dog Food 50#
16603 02021
Retriever Gravy Blend Dog Food 50#
49394 05665
Doggy Bag Dog Food 40#
73893 40000
Retriever Gravy Blend Dog Food 8#
79818 96756
Members Mark Complete Nutrition Premium Cat Food 20#
81131 89881
Retriever Hi Protein Dog Food 8#
79818 96755
Members Mark Complete Nutrition Premium Dog Food 50#
05388 67055
Retriever Hi Protein Dog Food 25#
49394 00002
Members Mark Crunchy Bites & Savory Bones Adult Dog Food 50#
05388 67309
Retriever Hi Protein Dog Food 50#
49394 00003
Members Mark High Performance Premium Dog Food 50#
81131 75479
Retriever Mini Chunk Dog Food 8#
79818 96754
Natural Cat Food (Sam's Club) 15#
81131 89883
Retriever Mini Chunk Dog Food 25#
49394 00006
Natural Dog Food (Sam's Club) 25#
81131 89884
Retriever Mini Chunk Dog Food 50#
49395 00005
Ol' Roy Complete Nutrition 4.4#
81131 69377
Retriever Puppy Blend Dog Food 6#
49394 56221
Ol' Roy Complete Nutrition 8#
05388 67144
Retriever Puppy Blend Dog Food 8#
79818 96758
Ol' Roy Complete Nutrition 22#
05388 60342
Retriever Puppy Blend Dog Food 20#
49394 00004
Ol' Roy Complete Nutrition 50#
78742 01022
Retriever Puppy Blend Dog Food 40#
79818 96706
Ol' Roy High Performance Nutrition Dog Food 20#
05388 60345
Special Kitty Gourmet 3.5#
81131 17546
Ol' Roy High Performance Nutrition Dog Food 50#
78742 05815
Special Kitty Gourmet 4#
78742 53199
Ol' Roy Meaty Chunks 'n Gravy Dog Food 8#
81131 69629
Special Kitty Gourmet 7#
81131 17547
Ol' Roy Meaty Chunks 'n Gravy Dog Food 22#
81131 69630
Special Kitty Gourmet 8#
78742 53200
Ol' Roy Meaty Chunks 'n Gravy Dog Food 50#
81131 69631
Special Kitty Gourmet 18#
81131 15748
Ol' Roy Puppy Complete 4#
81131 79078
Special Kitty Gourmet 20#
78742 53201
Ol' Roy Puppy Complete 8#
81131 79079
Special Kitty Gourmet 25#
78742 54314
Ol' Roy Puppy Complete 20#
81131 79080
Special Kitty Kitten 3.5#
81131 17553
Paws & Claws Delicious Mix Cat Food 8#
79818 96632
Special Kitty Kitten 4#
78742 53198
Paws & Claws Delicious Mix Cat Food 20#
49394 05746
Special Kitty Kitten 7#
81131 17554
Paws & Claws Delicious Mix Cat Food 40#
79818 96676
Special Kitty Kitten 8#
81131 24739
Paws & Claws Premium Choice Cat Food 8#
79818 96633
Special Kitty Original 3.5#
81131 17557
Paws & Claws Premium Choice Cat Food 20#
49394 00008
Special Kitty Original 4#
78742 04930
Paws & Claws Premium Choice Cat Food 40#
49394 05747
Special Kitty Original 7#
81131 17562
Pedigree Large Breed Adult Nutrition 20#
23100 29158
Special Kitty Original 8#
78742 05744
Pedigree Large Breed Adult Nutrition 30.1#
23100 31484
Special Kitty Original 18#
81131 17559
Pedigree Large Breed Adult Nutrition 36.4#
23100 31479
Special Kitty Original 20#
78742 05794
Pedigree Large Breed Adult Nutrition 40#
23100 29154
Special Kitty Original 25#
81131 68869
Pedigree Small Crunchy Bites Adult Nutrition 4.4#
23100 05104
Wegman's Bruiser Complete Nutrition Dog Food 4.4#
77890 33654
Pedigree Small Crunchy Bites Adult Nutrition 8.8#
23100 05103
Wegman's Bruiser Complete Nutrition Dog Food 20#
77890 32988
Pedigree Small Crunchy Bites Adult Nutrition 20#
23100 14719
Wegman's Bruiser Complete Nutrition Dog Food 37.5#
77890 32994
Pedigree Small Crunchy Bites Adult Nutrition 32#
23100 31483
Wegman's Bruiser Puppy Dog Food 4.4#
77890 33621
Pedigree Small Crunchy Bites Adult Nutrition 40#
23100 31478
Wegman's Bruiser Puppy Dog Food 17.6#
77890 32991
Pedigree Small Crunchy Bites Adult Nutrition 44#
23100 05100
Wegman's Bruiser Small Crunchy Bites Dog Food 4.4#
77890 33618
Pedigree Small Crunchy Bites Adult Nutrition 52#
23100 05110
Wegman's Bruiser Small Crunchy Bites Dog Food 20#
77890 32982
Pet Pride Indoor Cat 3.5#
11110 74584
Wegman's Buju & Ziggie Complete Cat Food 3.5#
77890 10005
Pet Pride Indoor Cat 18#
11110 74585
Wegman's Buju & Ziggie Complete Cat Food 18#
77890 10004
Pet Pride Weight Management Dog Food 17.6#
11110 74578
Wegman's Buju & Ziggie Indoor Cat Food 3.5#
77890 12038
PMI Nutrition Bites & Bones Dog Food 50#
42869 00174
Wegman's Buju & Ziggie Indoor Cat Food 18#
77890 12039
PMI Nutrition Canine Advantage 50#
42869 00172
Wegman's Buju & Ziggie Kitten 3.5#
77890 12036
PMI Nutrition Feline Medley 20#
42869 00171
Wegman's Buju & Ziggie Original Medley Cat Food 3.5#
77890 10006
PMI Nutrition Gravy Crunches Dog Food 40#
42869 00033
Wegman's Buju & Ziggie Original Medley Cat Food 18#
77890 10003
Red Flannel Active Formula Dog Food 40#
42869 00063
Red Flannel Adult Formula Dog Food 20#
42869 00055
Red Flannel Adult Formula Dog Food 40#
42869 00054
Red Flannel Canine Select Dog Food 20#
42869 00068
Red Flannel Canine Select Dog Food 40#
42869 00067
Red Flannel Cat 10#
42869 00059
Red Flannel Cat 20#
42869 00058
Red Flannel Hi Pro Formula Dog Food 50#
42869 00065
Red Flannel Prime Dog Food 25#
42869 00052
Red Flannel Prime Dog Food 50#
42869 00053
Red Flannel Puppy 40#
42869 00056
#
Mars Petcare Release (August 8, 2008)
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FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Mars Petcare US Issues Voluntary Recall of Everson, PA Plant Dry Pet Food Product due to Potential Salmonella Contamination
Contact:Debra Fair(973) 691-3536
FOR IMMEDIATE RELEASE -- Fanklin, Tennessee -- September 12, 2008 -- Today, Mars Petcare US announced a voluntary recall of products manufactured at its Everson, Pennsylvania facility. The pet food is being voluntarily recalled because of potential contamination with Salmonella serotypeSchwarzengrund. This voluntary recall only affects the United States.
Salmonella can cause serious infections in dogs and cats, and, if there is cross contamination caused by handling of the pet food, in people as well, especially children, the aged, and people with compromised immune systems. Healthy people potentially infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. On rare occasions, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.
Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Animals can be carriers with no visible symptoms and can potentially infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.
The company stopped production at the Everson facility on July 29, 2008 when it was alerted of a possible link between dry pet food produced at the plant and two isolated cases of people infected with Salmonella Schwarzengrund.
Even though no direct link between product produced at Everson and human or pet illness has been made, Mars Petcare US is taking precautionary action to protect pets and their owners by announcing a voluntary recall of all products produced at the Everson facility beginning February 18, 2008 until July 29, 2008 when we stopped production.
The company is continuing to work collaboratively with the FDA to determine the nature and source of Salmonella Schwarzengrund at the Everson facility. Since it has not yet identified the source of the Salmonella Schwarzengrund at the Everson facility, Mars Petcare US does not plan to resume production out of a commitment to the safety of our pet owners and their pets, customers, and associates.
The top priority of Mars Petcare US has always been and continues to be the health and welfare of pets and their owners. Consumers can continue to have confidence in the quality and safety of the products produced at other Mars Petcare US facilities. Only those products which were produced at the Everson facility are impacted by the voluntary recall.
Many of the brands involved in the recall are national brands produced at multiple facilities. A chart for all products is below. For example, PEDIGREE® is manufactured in numerous facilities throughout the country, and Everson represents a very small portion of the manufacturing base – 2.7 percent of total PEDIGREE® production.
Mars Petcare US will work with retail customers to ensure that the recalled products are not on store shelves. These products should not be sold or fed to pets. In the event that consumers believe they have purchased products affected by this voluntary recall, they should return the product to the store where they purchased it for a full refund. Specific product details and other information can be found at www.petcare.mars.com
Please find recalled pet food UPC information below.
The products listed below are made at our Everson facility on behalf of a variety of retailers. All code dates, with the exception of PEDIGREE®, are listed in a similar format as noted below:Consumers should look for “17” as the first two digits of the second line. Sample:Best By Feb 18 0917 1445 1
For PEDIGREE® the Everson code date format is as follows:
Consumers should look for “PAE” on the bottom line – the sixth, seventh and eighth digits. Sample:PEDIGREE ® Small Crunchy BitesBest Before 02/2009808G1PAE01 12:00
In an effort to prevent the transmission of Salmonella from pets to family members and care givers, the FDA recommends that everyone follow appropriate pet food handling guidelines when feeding their pets. A list of safe pet food handling tips can be found at: www.fda.gov/consumer/updates/petfoodtips080307.html
Pet owners who have questions about the recall should call 1-877-568-4463 or visit www.petcare.mars.com.
Recalled Pet Food Note: If you see a product you purchased listed below, please review the code date information samples from above to confirm that your product is included in the recall.
Product Name / Bag Size
UPC
Product Name / Bag Size
UPC
Country Acres Cat Food 40#
16603 02181
Retriever Bites & Bones Dog Food 8#
79818 96757
Country Acres Ration Dog Food 40#
16603 02333
Retriever Bites & Bones Dog Food 20#
79818 96634
Country Acres 18% Dog Food 40#
16603 02331
Retriever Bites & Bones Dog Food 50#
49394 05666
Country Acres Hi Pro Dog Food 50#
16603 02021
Retriever Gravy Blend Dog Food 50#
49394 05665
Doggy Bag Dog Food 40#
73893 40000
Retriever Gravy Blend Dog Food 8#
79818 96756
Members Mark Complete Nutrition Premium Cat Food 20#
81131 89881
Retriever Hi Protein Dog Food 8#
79818 96755
Members Mark Complete Nutrition Premium Dog Food 50#
05388 67055
Retriever Hi Protein Dog Food 25#
49394 00002
Members Mark Crunchy Bites & Savory Bones Adult Dog Food 50#
05388 67309
Retriever Hi Protein Dog Food 50#
49394 00003
Members Mark High Performance Premium Dog Food 50#
81131 75479
Retriever Mini Chunk Dog Food 8#
79818 96754
Natural Cat Food (Sam's Club) 15#
81131 89883
Retriever Mini Chunk Dog Food 25#
49394 00006
Natural Dog Food (Sam's Club) 25#
81131 89884
Retriever Mini Chunk Dog Food 50#
49395 00005
Ol' Roy Complete Nutrition 4.4#
81131 69377
Retriever Puppy Blend Dog Food 6#
49394 56221
Ol' Roy Complete Nutrition 8#
05388 67144
Retriever Puppy Blend Dog Food 8#
79818 96758
Ol' Roy Complete Nutrition 22#
05388 60342
Retriever Puppy Blend Dog Food 20#
49394 00004
Ol' Roy Complete Nutrition 50#
78742 01022
Retriever Puppy Blend Dog Food 40#
79818 96706
Ol' Roy High Performance Nutrition Dog Food 20#
05388 60345
Special Kitty Gourmet 3.5#
81131 17546
Ol' Roy High Performance Nutrition Dog Food 50#
78742 05815
Special Kitty Gourmet 4#
78742 53199
Ol' Roy Meaty Chunks 'n Gravy Dog Food 8#
81131 69629
Special Kitty Gourmet 7#
81131 17547
Ol' Roy Meaty Chunks 'n Gravy Dog Food 22#
81131 69630
Special Kitty Gourmet 8#
78742 53200
Ol' Roy Meaty Chunks 'n Gravy Dog Food 50#
81131 69631
Special Kitty Gourmet 18#
81131 15748
Ol' Roy Puppy Complete 4#
81131 79078
Special Kitty Gourmet 20#
78742 53201
Ol' Roy Puppy Complete 8#
81131 79079
Special Kitty Gourmet 25#
78742 54314
Ol' Roy Puppy Complete 20#
81131 79080
Special Kitty Kitten 3.5#
81131 17553
Paws & Claws Delicious Mix Cat Food 8#
79818 96632
Special Kitty Kitten 4#
78742 53198
Paws & Claws Delicious Mix Cat Food 20#
49394 05746
Special Kitty Kitten 7#
81131 17554
Paws & Claws Delicious Mix Cat Food 40#
79818 96676
Special Kitty Kitten 8#
81131 24739
Paws & Claws Premium Choice Cat Food 8#
79818 96633
Special Kitty Original 3.5#
81131 17557
Paws & Claws Premium Choice Cat Food 20#
49394 00008
Special Kitty Original 4#
78742 04930
Paws & Claws Premium Choice Cat Food 40#
49394 05747
Special Kitty Original 7#
81131 17562
Pedigree Large Breed Adult Nutrition 20#
23100 29158
Special Kitty Original 8#
78742 05744
Pedigree Large Breed Adult Nutrition 30.1#
23100 31484
Special Kitty Original 18#
81131 17559
Pedigree Large Breed Adult Nutrition 36.4#
23100 31479
Special Kitty Original 20#
78742 05794
Pedigree Large Breed Adult Nutrition 40#
23100 29154
Special Kitty Original 25#
81131 68869
Pedigree Small Crunchy Bites Adult Nutrition 4.4#
23100 05104
Wegman's Bruiser Complete Nutrition Dog Food 4.4#
77890 33654
Pedigree Small Crunchy Bites Adult Nutrition 8.8#
23100 05103
Wegman's Bruiser Complete Nutrition Dog Food 20#
77890 32988
Pedigree Small Crunchy Bites Adult Nutrition 20#
23100 14719
Wegman's Bruiser Complete Nutrition Dog Food 37.5#
77890 32994
Pedigree Small Crunchy Bites Adult Nutrition 32#
23100 31483
Wegman's Bruiser Puppy Dog Food 4.4#
77890 33621
Pedigree Small Crunchy Bites Adult Nutrition 40#
23100 31478
Wegman's Bruiser Puppy Dog Food 17.6#
77890 32991
Pedigree Small Crunchy Bites Adult Nutrition 44#
23100 05100
Wegman's Bruiser Small Crunchy Bites Dog Food 4.4#
77890 33618
Pedigree Small Crunchy Bites Adult Nutrition 52#
23100 05110
Wegman's Bruiser Small Crunchy Bites Dog Food 20#
77890 32982
Pet Pride Indoor Cat 3.5#
11110 74584
Wegman's Buju & Ziggie Complete Cat Food 3.5#
77890 10005
Pet Pride Indoor Cat 18#
11110 74585
Wegman's Buju & Ziggie Complete Cat Food 18#
77890 10004
Pet Pride Weight Management Dog Food 17.6#
11110 74578
Wegman's Buju & Ziggie Indoor Cat Food 3.5#
77890 12038
PMI Nutrition Bites & Bones Dog Food 50#
42869 00174
Wegman's Buju & Ziggie Indoor Cat Food 18#
77890 12039
PMI Nutrition Canine Advantage 50#
42869 00172
Wegman's Buju & Ziggie Kitten 3.5#
77890 12036
PMI Nutrition Feline Medley 20#
42869 00171
Wegman's Buju & Ziggie Original Medley Cat Food 3.5#
77890 10006
PMI Nutrition Gravy Crunches Dog Food 40#
42869 00033
Wegman's Buju & Ziggie Original Medley Cat Food 18#
77890 10003
Red Flannel Active Formula Dog Food 40#
42869 00063
Red Flannel Adult Formula Dog Food 20#
42869 00055
Red Flannel Adult Formula Dog Food 40#
42869 00054
Red Flannel Canine Select Dog Food 20#
42869 00068
Red Flannel Canine Select Dog Food 40#
42869 00067
Red Flannel Cat 10#
42869 00059
Red Flannel Cat 20#
42869 00058
Red Flannel Hi Pro Formula Dog Food 50#
42869 00065
Red Flannel Prime Dog Food 25#
42869 00052
Red Flannel Prime Dog Food 50#
42869 00053
Red Flannel Puppy 40#
42869 00056
#
Mars Petcare Release (August 8, 2008)
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Monday, September 8, 2008
T Marzetti Company Announces Limited Recall of Girard's Honey Dijon Peppercorn Salad Dressing
September 5, 2008
T Marzetti Company Announces Limited Recall of Girard's Honey Dijon Peppercorn Salad Dressing
Arlington VA -- T. Marzetti Company, Columbus, Ohio is recalling a limited number of 12 fl. oz. bottles of Girard's Honey Dijon Peppercorn (item 58105) because they may have the incorrect back label of Girard's French Dressing (item 58015). The Girard's Honey Dijon Peppercorn contains eggs, which is not declared as an ingredient on the Girard's French label. People who have allergies to egg run the risk of serious allergic reaction if they consume this product.
The bottles were shipped in corrugated cases marked with the item number 58105 and with a date code of Best By 06-11-09M. The 12 fl. oz. bottles are labeled with "Girard's Honey Dijon Peppercorn" on the front, the back of the bottle may be labeled with Girard's French Dressing (item 58015), with the date code of Best By 06-11-09M. No other date codes are involved in the recall.
The recalled bottles of Girard's Honey Dijon Peppercorn Dressing were distributed throughout the western United States (primarily California, Washington, Oregon and Arizona).
No illnesses have been reported in connection with this problem.
Consumers who have purchased 12 fl. oz. bottles of Girard's Honey Dijon Peppercorn with the incorrect back label are urged to return them to the place of purchase for a full refund. Anyone with questions may contact the company's consumer response department at 614-846-2232.
T Marzetti Company Announces Limited Recall of Girard's Honey Dijon Peppercorn Salad Dressing
Arlington VA -- T. Marzetti Company, Columbus, Ohio is recalling a limited number of 12 fl. oz. bottles of Girard's Honey Dijon Peppercorn (item 58105) because they may have the incorrect back label of Girard's French Dressing (item 58015). The Girard's Honey Dijon Peppercorn contains eggs, which is not declared as an ingredient on the Girard's French label. People who have allergies to egg run the risk of serious allergic reaction if they consume this product.
The bottles were shipped in corrugated cases marked with the item number 58105 and with a date code of Best By 06-11-09M. The 12 fl. oz. bottles are labeled with "Girard's Honey Dijon Peppercorn" on the front, the back of the bottle may be labeled with Girard's French Dressing (item 58015), with the date code of Best By 06-11-09M. No other date codes are involved in the recall.
The recalled bottles of Girard's Honey Dijon Peppercorn Dressing were distributed throughout the western United States (primarily California, Washington, Oregon and Arizona).
No illnesses have been reported in connection with this problem.
Consumers who have purchased 12 fl. oz. bottles of Girard's Honey Dijon Peppercorn with the incorrect back label are urged to return them to the place of purchase for a full refund. Anyone with questions may contact the company's consumer response department at 614-846-2232.
The Hershey Co. recalls 7.25-ounce plastic Bottles of Hershey's Chocolate Shell Topping
September 5, 2008
Second Update: The Hershey Co. recalls 7.25-ounce plastic Bottles of Hershey's Chocolate Shell Topping
Arlington VA -- The Hershey Co. is recalling : Hershey’s Chocolate Shell Topping, 7.25-ounce bottles (consumer units only) Code 69N, which are packed in master cases of Heath Shell Topping Code 69N, the ice cream topping contains undeclared almonds, which could cause a severe or life-threatening reaction in people who have allergies to almonds.
A small portion of a Heath Shell Topping production run used bottles labeled HERSHEY’S Chocolate Shell Topping. This resulted in a small number of the Heath master cases containing both Hershey’s Chocolate Shell and Heath Shell Topping bottles
The Hershey, Pa., company has heard three consumer complaints. There have been no reports of incidents or injuries.
The product, with the UPC/bar code 346000, was sold nationwide after July 8 this year.
Second Update: The Hershey Co. recalls 7.25-ounce plastic Bottles of Hershey's Chocolate Shell Topping
Arlington VA -- The Hershey Co. is recalling : Hershey’s Chocolate Shell Topping, 7.25-ounce bottles (consumer units only) Code 69N, which are packed in master cases of Heath Shell Topping Code 69N, the ice cream topping contains undeclared almonds, which could cause a severe or life-threatening reaction in people who have allergies to almonds.
A small portion of a Heath Shell Topping production run used bottles labeled HERSHEY’S Chocolate Shell Topping. This resulted in a small number of the Heath master cases containing both Hershey’s Chocolate Shell and Heath Shell Topping bottles
The Hershey, Pa., company has heard three consumer complaints. There have been no reports of incidents or injuries.
The product, with the UPC/bar code 346000, was sold nationwide after July 8 this year.
Friday, September 5, 2008
STARWAY INC. ISSUES ALERT ON
S T A R W A Y I N C.
137 Grattan Street
BROOKLYN, NEW YORK 11237
Tel.: 718-417-1788 Fax: 718-417-1983
September 3, 2008
FOR IMMEDIATE RELEASE
Contact Person: Chris Lee
Telephone No.: 718-417-1788
STARWAY INC. ISSUES ALERT ON
UNDECLARED SULFITES IN EGO BRAND PRESERVED PEACHES
Starway Incorporated, located at 137 Grattan Street, Brooklyn, NY, 11237, is recalling EGO brand Preserved Peaches because the product contains undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product.
EGO brand Preserved Peaches is sold in a 14 ounce, un-coded, clear plastic package and was distributed nationwide. It is a product of Malaysia.
The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the presence of sulfites in EGO brand Preserved Peaches which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date in connection with this problem.
Consumers who have purchased EGO brand Preserved Peaches are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 718-417-1788.
137 Grattan Street
BROOKLYN, NEW YORK 11237
Tel.: 718-417-1788 Fax: 718-417-1983
September 3, 2008
FOR IMMEDIATE RELEASE
Contact Person: Chris Lee
Telephone No.: 718-417-1788
STARWAY INC. ISSUES ALERT ON
UNDECLARED SULFITES IN EGO BRAND PRESERVED PEACHES
Starway Incorporated, located at 137 Grattan Street, Brooklyn, NY, 11237, is recalling EGO brand Preserved Peaches because the product contains undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product.
EGO brand Preserved Peaches is sold in a 14 ounce, un-coded, clear plastic package and was distributed nationwide. It is a product of Malaysia.
The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the presence of sulfites in EGO brand Preserved Peaches which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date in connection with this problem.
Consumers who have purchased EGO brand Preserved Peaches are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 718-417-1788.
Wednesday, September 3, 2008
STARWAY INC. ISSUES ALERT ON
S T A R W A Y I N C.
137 Grattan Street
BROOKLYN, NEW YORK 11237
Tel.: 718-417-1788 Fax: 718-417-1983
September 3, 2008
FOR IMMEDIATE RELEASE
Contact Person: Chris Lee
Telephone No.: 718-417-1788
STARWAY INC. ISSUES ALERT ON
UNDECLARED SULFITES IN EGO BRAND PRESERVED PEACHES
Starway Incorporated, located at 137 Grattan Street, Brooklyn, NY, 11237, is recalling EGO brand Preserved Peaches because the product contains undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product.
EGO brand Preserved Peaches is sold in a 14 ounce, un-coded, clear plastic package and was distributed nationwide. It is a product of Malaysia.
The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the presence of sulfites in EGO brand Preserved Peaches which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date in connection with this problem.
Consumers who have purchased EGO brand Preserved Peaches are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 718-417-1788.
137 Grattan Street
BROOKLYN, NEW YORK 11237
Tel.: 718-417-1788 Fax: 718-417-1983
September 3, 2008
FOR IMMEDIATE RELEASE
Contact Person: Chris Lee
Telephone No.: 718-417-1788
STARWAY INC. ISSUES ALERT ON
UNDECLARED SULFITES IN EGO BRAND PRESERVED PEACHES
Starway Incorporated, located at 137 Grattan Street, Brooklyn, NY, 11237, is recalling EGO brand Preserved Peaches because the product contains undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product.
EGO brand Preserved Peaches is sold in a 14 ounce, un-coded, clear plastic package and was distributed nationwide. It is a product of Malaysia.
The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the presence of sulfites in EGO brand Preserved Peaches which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date in connection with this problem.
Consumers who have purchased EGO brand Preserved Peaches are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 718-417-1788.
Thursday, August 28, 2008
Bailey’s Crab & Oysters, Port Norris, New Jersey (NJ 89 SS) has initiated a voluntary recall of oyster shell stock
EHS Circular Letter #2008-68
To: Local Directors of Health
Chief Sanitarians
Certified Food Inspectors
From: Tracey Weeks, MS, RS; Food Protection Program
Date: August 26, 2008
Subject: Oyster Recall by a New Jersey Firm
Bailey’s Crab & Oysters, Port Norris, New Jersey (NJ 89 SS) has initiated a voluntary recall of oyster shell stock. The recall was initiated because of two confirmed cases of Vibrio parahaemolyticus associated with product harvested from “Ship John” and “Shell Rock” New Jersey growing areas on July 14-15, 2008 and shipped by Bailey’s Crabs & Oysters from July 7, 2008 to August 19, 2008.
According to the Connecticut Department of Agriculture, Bureau of Aquaculture, to date, the Connecticut shellfish dealers have not reported Connecticut distribution of the recalled oysters.
Please refer to the attached recall notice for specific product information. If you encounter any of the recalled product you are advised to embargo it and contact James Citak at the Connecticut Department of Agriculture, Bureau of Aquaculture, (203) 874-0696 for information on proper disposition.
To: Local Directors of Health
Chief Sanitarians
Certified Food Inspectors
From: Tracey Weeks, MS, RS; Food Protection Program
Date: August 26, 2008
Subject: Oyster Recall by a New Jersey Firm
Bailey’s Crab & Oysters, Port Norris, New Jersey (NJ 89 SS) has initiated a voluntary recall of oyster shell stock. The recall was initiated because of two confirmed cases of Vibrio parahaemolyticus associated with product harvested from “Ship John” and “Shell Rock” New Jersey growing areas on July 14-15, 2008 and shipped by Bailey’s Crabs & Oysters from July 7, 2008 to August 19, 2008.
According to the Connecticut Department of Agriculture, Bureau of Aquaculture, to date, the Connecticut shellfish dealers have not reported Connecticut distribution of the recalled oysters.
Please refer to the attached recall notice for specific product information. If you encounter any of the recalled product you are advised to embargo it and contact James Citak at the Connecticut Department of Agriculture, Bureau of Aquaculture, (203) 874-0696 for information on proper disposition.
Tuesday, August 26, 2008
NJ Department of Health and Senior Services (NJDHSS) is informing you with information on a Firm-Initiated Recall of oyster shellstock.
NEW JERSEY DEPARTMENT OF HEALTH AND SENIOR SERVICES
ATTENTION: REVISED CLASS 1 – FIRM-INITIATED VOLUNTARY RECALL The NJ Department of Health and Senior Services (NJDHSS) is informing you with information on a Firm-Initiated Recall of oyster shellstock. Bailey’s Crabs & Oysters of Port Norris, New Jersey (NJ 89 SS) has initiated a voluntary recall for all product shipped from July 7, 2008 to August 19, 2008. The cause of this action is two confirmed cases (1 MD, 1 DE) of Vibrio parahaemolyticus – associated illnesses from two different NJ growing areas (Ship John and Shell Rock -harvest dates July14, 2008 - July 15, 2008 both areas/dates) implicated to product harvested and shipped by this dealer. At present we are aware of oysters going to the following states and the following first dealers: Delivered to Fulton Market, Bronx, NY - Food Center Dr., Booth # • Alaskan Feast - 120 boxes • Blue Ribbon - 180 boxes • Lockwood & Winant - 120 boxes • Monarch Seafood (NJ) - 95 boxes • New Seafood - 230 boxes Delivered to ACA, Bronx, NY • Di Martino's - 80 boxes • K&B Seafood - 110 boxes Delivered to Illinois by common carrier - Amory • Boston Fish - 60 boxes • Blue Marlin - 232 boxes • Eastern Seafood - 90 boxes • Gold Star - 120 boxes • Rubino's - 273 boxes • Superior Lobster - 519 boxes • Supreme Fish - 20 boxes Delivered to St. Louis, MO • Fabulous Fish - 134 boxes Delivered to Milwaukee, WI • St. Paul Fish - 66 boxes
Delivered to Maryland • Harris Seafood (Primary wholesaler) - 1030 bushels and 76 bags • Chester River Clam Company (Secondary wholesaler) Delivered to VA • Roy Davis - 383 boxes • Bevins - 10 boxes (? amount was difficult to read, check invoice) Delivered to NJ • Trinity Seafood - 47 boxes • Peter McCarthy - 69 boxes • Parsons - 40 boxes Should you observe any of the implicated product from July 7, 2008 - August 19, 2008 please embargo and contact the owner of Bailey's Crabs and Oysters - Scott Bailey at 856-785-0025. The NJDHSS has been in contact the US Food and Drug Administration Regional Shellfish Specialist and per this email all the receiving states. If you need any further information please contact Cali Alexander - NJDHSS Seafood/Shellfish Coordinator 609-588-3123. Please be advised that the above Class 1 Voluntary Firm Recall is based on the best available information provided to the NJDHSS - Food and Drug Safety Program to date. Per discussions with the USFDA, you are being advised immediately of this expanded recall. Harvesting from these waters has been temporarily suspended until further notice while the NJDEP performs testing for Vibrio parahaemolyticus levels in oysters from the implicated shellfish beds. If you need further information on this harvest suspension, please contact Bob Connell - NJDEP Bureau of Water Monitoring - 609-748-2000.
ATTENTION: REVISED CLASS 1 – FIRM-INITIATED VOLUNTARY RECALL The NJ Department of Health and Senior Services (NJDHSS) is informing you with information on a Firm-Initiated Recall of oyster shellstock. Bailey’s Crabs & Oysters of Port Norris, New Jersey (NJ 89 SS) has initiated a voluntary recall for all product shipped from July 7, 2008 to August 19, 2008. The cause of this action is two confirmed cases (1 MD, 1 DE) of Vibrio parahaemolyticus – associated illnesses from two different NJ growing areas (Ship John and Shell Rock -harvest dates July14, 2008 - July 15, 2008 both areas/dates) implicated to product harvested and shipped by this dealer. At present we are aware of oysters going to the following states and the following first dealers: Delivered to Fulton Market, Bronx, NY - Food Center Dr., Booth # • Alaskan Feast - 120 boxes • Blue Ribbon - 180 boxes • Lockwood & Winant - 120 boxes • Monarch Seafood (NJ) - 95 boxes • New Seafood - 230 boxes Delivered to ACA, Bronx, NY • Di Martino's - 80 boxes • K&B Seafood - 110 boxes Delivered to Illinois by common carrier - Amory • Boston Fish - 60 boxes • Blue Marlin - 232 boxes • Eastern Seafood - 90 boxes • Gold Star - 120 boxes • Rubino's - 273 boxes • Superior Lobster - 519 boxes • Supreme Fish - 20 boxes Delivered to St. Louis, MO • Fabulous Fish - 134 boxes Delivered to Milwaukee, WI • St. Paul Fish - 66 boxes
Delivered to Maryland • Harris Seafood (Primary wholesaler) - 1030 bushels and 76 bags • Chester River Clam Company (Secondary wholesaler) Delivered to VA • Roy Davis - 383 boxes • Bevins - 10 boxes (? amount was difficult to read, check invoice) Delivered to NJ • Trinity Seafood - 47 boxes • Peter McCarthy - 69 boxes • Parsons - 40 boxes Should you observe any of the implicated product from July 7, 2008 - August 19, 2008 please embargo and contact the owner of Bailey's Crabs and Oysters - Scott Bailey at 856-785-0025. The NJDHSS has been in contact the US Food and Drug Administration Regional Shellfish Specialist and per this email all the receiving states. If you need any further information please contact Cali Alexander - NJDHSS Seafood/Shellfish Coordinator 609-588-3123. Please be advised that the above Class 1 Voluntary Firm Recall is based on the best available information provided to the NJDHSS - Food and Drug Safety Program to date. Per discussions with the USFDA, you are being advised immediately of this expanded recall. Harvesting from these waters has been temporarily suspended until further notice while the NJDEP performs testing for Vibrio parahaemolyticus levels in oysters from the implicated shellfish beds. If you need further information on this harvest suspension, please contact Bob Connell - NJDEP Bureau of Water Monitoring - 609-748-2000.
Monday, August 25, 2008
Nestlé USA is announcing a product recall on our Hot Pockets Pepperoni Pizza Club Pack 6(12 x 4.5oz
Nestlé USA is announcing a product recall on our Hot Pockets Pepperoni Pizza Club Pack 6(12 x 4.5oz). This retrieval is due to the possibility that plastic pieces may be in the product.
Please communicate to your Distribution Center(s) and retail outlets alerting them to the details of this recall and direct them to remove product of the affected items with the Batch Code listed below.
Customers may see a batch code of 8157544618E. This product was made on a different production line and is NOT TO BE REMOVED FROM INVENTORY
NO LEAN POCKETS® brand items and NO other HOT POCKETS® brand items, including 2 and 5 pk Pepperoni Pizza, are affected by this recall.
Your assistance is greatly appreciated in clearing warehouses, storage rooms, and store shelves of this potentially affected product.
Warehouse inventory of affected product subject to this recall should be returned. If 50 cases or fewer are in the warehouse, you can destroy the product on site and provide documentation for reimbursement. Please provide your Nestlé Representative with a signed statement which details the case quantity destroyed by SKU. If product is destroyed, you are required to provide a signed statement and Certificate of Destruction (COD) as to the number of cases physically destroyed. The Account Order Coordinator will need the COD in order to process the appropriate credit.
Please notify all retail stores serviced and instruct them to pull all affected product listed above and destroy the product. Retail locations must provide documentation indicating the quantity of product destroyed. Retail outlets supplied by distributors must identify the product supplier as well. The appropriate documentation should be e-mailed to David Kochems (david.kochems@us.nestle.com) or faxed to Glendale 818-549-6399 attention of David Kochems.
Please contact your Nestlé Sales Representative, if you have any questions.
We apologize for any inconvenience this may cause and thank you in advance for your cooperation.
Please communicate to your Distribution Center(s) and retail outlets alerting them to the details of this recall and direct them to remove product of the affected items with the Batch Code listed below.
Customers may see a batch code of 8157544618E. This product was made on a different production line and is NOT TO BE REMOVED FROM INVENTORY
NO LEAN POCKETS® brand items and NO other HOT POCKETS® brand items, including 2 and 5 pk Pepperoni Pizza, are affected by this recall.
Your assistance is greatly appreciated in clearing warehouses, storage rooms, and store shelves of this potentially affected product.
Warehouse inventory of affected product subject to this recall should be returned. If 50 cases or fewer are in the warehouse, you can destroy the product on site and provide documentation for reimbursement. Please provide your Nestlé Representative with a signed statement which details the case quantity destroyed by SKU. If product is destroyed, you are required to provide a signed statement and Certificate of Destruction (COD) as to the number of cases physically destroyed. The Account Order Coordinator will need the COD in order to process the appropriate credit.
Please notify all retail stores serviced and instruct them to pull all affected product listed above and destroy the product. Retail locations must provide documentation indicating the quantity of product destroyed. Retail outlets supplied by distributors must identify the product supplier as well. The appropriate documentation should be e-mailed to David Kochems (david.kochems@us.nestle.com) or faxed to Glendale 818-549-6399 attention of David Kochems.
Please contact your Nestlé Sales Representative, if you have any questions.
We apologize for any inconvenience this may cause and thank you in advance for your cooperation.
Friday, August 22, 2008
Nebraska Firm Expands Recall of Beef Products Due To Possible E. Coli O157:H7 Contamination
Nebraska Firm Expands Recall of Beef Products Due To Possible E. Coli O157:H7 Contamination
Nebraska Beef, Ltd., an Omaha, Neb., establishment, is clarifying information from and expanding its recall announced on Aug. 8 of primal cuts, subprimal cuts and boxed beef to include such products bearing the company name "Nebraska Beef Ltd" that may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture's Food Safety and Inspection Service announced today. The total amount of product subject to recall is approximately 1.36 million pounds. The expansion of approximately 160,000 pounds and the clarifying information include:
Primal cuts, subprimal cuts and boxed beef produced on June 24, whose shipping containers and labels bear the establishment number "EST. 19336" inside the USDA mark of inspection and the company name "Nebraska Beef Ltd" The products may or may not bear a green sticker.
Primal cuts, subprimal cuts and boxed beef produced on July 8, whose shipping containers and labels bear the establishment number "EST. 19336" inside the USDA mark of inspection, the company name "Nebraska Beef Ltd." as well as a 2-inch plain, circular green sticker on one side of the shipping box.
Poundage of products bearing the green sticker were included in the 1.2 million pounds originally recalled, but were not identified in the product description with the company name "Nebraska Beef Ltd." in the Aug. 8 announcement. FSIS has concluded that the production practices employed by Nebraska Beef, Ltd., on June 24 were insufficient to effectively control E. coli O157:H7. The products subject to the expansion may have been produced under insanitary conditions. The expansion was not prompted by foodborne illness investigations. These products were sent to establishments and retail stores nationwide for further processing and will likely not bear the establishment number "EST. 19336" on products available for direct consumer purchase. Consumers with questions about the recall should contact company Vice President of Administration James Timmerman at 402-733-0456. Media with questions about the recall should contact company representative William Lamson at (402) 397-7300. The problem prompting the recall announced on Aug. 8 was discovered through a joint investigation with state departments of health and agriculture, the Centers for Disease Control and Prevention and FSIS. As of Aug. 11, there were 26 culture-confirmed cases in 10 states and 1 culture-confirmed case in Canada identified as part of this outbreak. This count is based on continuing testing, analysis and investigation. SIS is continuing its investigation into any products that may be contaminated with E. coli O157:H7 or that are associated with illnesses and will take appropriate action when necessary. E. coli O157:H7 is a potentially deadly bacterium that can cause bloody diarrhea, dehydration, and in the most severe cases, kidney failure. The very young, seniors and persons with weak immune systems are the most susceptible to foodborne illness. Anyone with signs or symptoms of foodborne illness should consult a medical professional (USDA.gov).
Nebraska Beef, Ltd., an Omaha, Neb., establishment, is clarifying information from and expanding its recall announced on Aug. 8 of primal cuts, subprimal cuts and boxed beef to include such products bearing the company name "Nebraska Beef Ltd" that may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture's Food Safety and Inspection Service announced today. The total amount of product subject to recall is approximately 1.36 million pounds. The expansion of approximately 160,000 pounds and the clarifying information include:
Primal cuts, subprimal cuts and boxed beef produced on June 24, whose shipping containers and labels bear the establishment number "EST. 19336" inside the USDA mark of inspection and the company name "Nebraska Beef Ltd" The products may or may not bear a green sticker.
Primal cuts, subprimal cuts and boxed beef produced on July 8, whose shipping containers and labels bear the establishment number "EST. 19336" inside the USDA mark of inspection, the company name "Nebraska Beef Ltd." as well as a 2-inch plain, circular green sticker on one side of the shipping box.
Poundage of products bearing the green sticker were included in the 1.2 million pounds originally recalled, but were not identified in the product description with the company name "Nebraska Beef Ltd." in the Aug. 8 announcement. FSIS has concluded that the production practices employed by Nebraska Beef, Ltd., on June 24 were insufficient to effectively control E. coli O157:H7. The products subject to the expansion may have been produced under insanitary conditions. The expansion was not prompted by foodborne illness investigations. These products were sent to establishments and retail stores nationwide for further processing and will likely not bear the establishment number "EST. 19336" on products available for direct consumer purchase. Consumers with questions about the recall should contact company Vice President of Administration James Timmerman at 402-733-0456. Media with questions about the recall should contact company representative William Lamson at (402) 397-7300. The problem prompting the recall announced on Aug. 8 was discovered through a joint investigation with state departments of health and agriculture, the Centers for Disease Control and Prevention and FSIS. As of Aug. 11, there were 26 culture-confirmed cases in 10 states and 1 culture-confirmed case in Canada identified as part of this outbreak. This count is based on continuing testing, analysis and investigation. SIS is continuing its investigation into any products that may be contaminated with E. coli O157:H7 or that are associated with illnesses and will take appropriate action when necessary. E. coli O157:H7 is a potentially deadly bacterium that can cause bloody diarrhea, dehydration, and in the most severe cases, kidney failure. The very young, seniors and persons with weak immune systems are the most susceptible to foodborne illness. Anyone with signs or symptoms of foodborne illness should consult a medical professional (USDA.gov).
NESTLE RECALLS Pepperoni HOT POCKETS That May Contain Foreign Mate
NESTLE RECALLS Pepperoni HOT POCKETS That May Contain Foreign Materials
Recall Release
CLASS I RECALL
FSIS-RC-033-2008
HEALTH RISK: HIGH
Congressional and Public Affairs (202) 720-9113Peggy Riek
WASHINGTON, Aug. 21, 2008 - Nestlé Prepared Foods Company, a Mt. Sterling, Ky., establishment, is recalling approximately 215,660 pounds of frozen stuffed pepperoni pizza sandwich products that may contain foreign materials, the U.S. Department of Agriculture's Food Safety and Inspection Service announced today. The following products are subject to recall:
54-ounce, 12-pack cartons of "HOT POCKETS PEPPERONI PIZZA" brand stuffed sandwiches. Printed on the side of each carton is "8157544614D," "EST 7721A," and "BEST BEFORE JAN2010." Each carton bears the USDA mark of inspection.
The products were produced on June 5 and distributed to retail establishments nationwide. The problem was discovered after the company received consumer complaints. FSIS has not received any consumer complaints or reports of injury at this time. Anyone concerned about an injury from consumption of the products should contact a physician (USDA).
Recall Release
CLASS I RECALL
FSIS-RC-033-2008
HEALTH RISK: HIGH
Congressional and Public Affairs (202) 720-9113Peggy Riek
WASHINGTON, Aug. 21, 2008 - Nestlé Prepared Foods Company, a Mt. Sterling, Ky., establishment, is recalling approximately 215,660 pounds of frozen stuffed pepperoni pizza sandwich products that may contain foreign materials, the U.S. Department of Agriculture's Food Safety and Inspection Service announced today. The following products are subject to recall:
54-ounce, 12-pack cartons of "HOT POCKETS PEPPERONI PIZZA" brand stuffed sandwiches. Printed on the side of each carton is "8157544614D," "EST 7721A," and "BEST BEFORE JAN2010." Each carton bears the USDA mark of inspection.
The products were produced on June 5 and distributed to retail establishments nationwide. The problem was discovered after the company received consumer complaints. FSIS has not received any consumer complaints or reports of injury at this time. Anyone concerned about an injury from consumption of the products should contact a physician (USDA).
Thursday, August 7, 2008
Mississippi Firm Recalls Chicken Breast Products
August 7, 2008
Mississippi Firm Recalls Chicken Breast Products
Due To Undeclared Allergens
Arlington, VA – Tyson Foods, Inc., a Vicksburg, Mississippi establishment, is recalling approximately 51,360 pounds of raw frozen chicken breast tenderloin products because they may contain an undeclared allergen, soy, the U. S. Department of Agriculture’s Food Safety and Inspection Service announced today. The products contain soy, a known allergen, which is not declared on the label.
The following products are subject to recall:
10-pound cases of “Standard Quality Uncooked Fritters, Old Fashioned Chicken Breast Tenderloins.” Each box bears the case code of “2523-954” as well as a packaging date of “7/23/08” printed on the side of the box.
10-pound cases of “Sysco Uncooked, Fritters, Chicken Breast Tenderloins.” Each box bears the case code of “2523-895” as well as packaging dates of “7/24/08” or “7/29/08” printed on the side of the box.
10-pound cases of “Heritage Valley Uncooked Steakhouse Chicken Breast Tenderloin Fritters.” Each box bears the case code of “2523-398” as well as a packaging date of “7/23/08”, “7/24/08,” or “8/01/08” printed on the side of the box.
20-pound cases of “Spare Time Uncooked Fritters, Chicken Breast Tenderloins.” Each box bears the case code of “2523-861” as well as a packaging date of “7/23/08” printed on the side of the box.
10-pound cases of “Tyson Uncooked Chicken Breast Tenderloin Fritters.” Each box bears the code of “2989-928” as well as a packaging date of “7/25/08” printed on the side of the box.
The chicken breast tenderloin products were produced between July 23 and August 1, 2008 and were shipped to Tyson food service distributors nationwide.
The problem was discovered by the company. FSIS has received no reports of illness due to consumption of these products. Anyone concerned about an allergic reaction should contact a physician.
Consumers with questions about the recall should contact company Manager of Consumer Relations Willie Barber at (866) 328-3156.
Mississippi Firm Recalls Chicken Breast Products
Due To Undeclared Allergens
Arlington, VA – Tyson Foods, Inc., a Vicksburg, Mississippi establishment, is recalling approximately 51,360 pounds of raw frozen chicken breast tenderloin products because they may contain an undeclared allergen, soy, the U. S. Department of Agriculture’s Food Safety and Inspection Service announced today. The products contain soy, a known allergen, which is not declared on the label.
The following products are subject to recall:
10-pound cases of “Standard Quality Uncooked Fritters, Old Fashioned Chicken Breast Tenderloins.” Each box bears the case code of “2523-954” as well as a packaging date of “7/23/08” printed on the side of the box.
10-pound cases of “Sysco Uncooked, Fritters, Chicken Breast Tenderloins.” Each box bears the case code of “2523-895” as well as packaging dates of “7/24/08” or “7/29/08” printed on the side of the box.
10-pound cases of “Heritage Valley Uncooked Steakhouse Chicken Breast Tenderloin Fritters.” Each box bears the case code of “2523-398” as well as a packaging date of “7/23/08”, “7/24/08,” or “8/01/08” printed on the side of the box.
20-pound cases of “Spare Time Uncooked Fritters, Chicken Breast Tenderloins.” Each box bears the case code of “2523-861” as well as a packaging date of “7/23/08” printed on the side of the box.
10-pound cases of “Tyson Uncooked Chicken Breast Tenderloin Fritters.” Each box bears the code of “2989-928” as well as a packaging date of “7/25/08” printed on the side of the box.
The chicken breast tenderloin products were produced between July 23 and August 1, 2008 and were shipped to Tyson food service distributors nationwide.
The problem was discovered by the company. FSIS has received no reports of illness due to consumption of these products. Anyone concerned about an allergic reaction should contact a physician.
Consumers with questions about the recall should contact company Manager of Consumer Relations Willie Barber at (866) 328-3156.
raw oysters labeled “For Cooking Only”
To Retail Food Regulatory Agencies:
We are providing the following information to you in advance of its delivery to the retail food trade organizations and asking your assistance in advising food establishments that raw oysters labeled “For Cooking Only” should not be sold or served to consumers in the raw form. FDA expects this “For Cooking Only” labeling as a control for the reduction of risk associated with Vibrio parahaemolyticus in oysters to be a temporary measure.
We are asking your assistance to help provide the attached information to retailers and restaurateurs who serve or sell raw oysters. If possible, please forward this advice to your organization’s members and to your state affiliate organizations as well. Certain states are requiring some shipments of oysters be labeled “For Cooking Only” as part of their Vibrio parahaemolyticus Control Plan under the National Shellfish Sanitation Program (NSSP).
This attachment explains what that means and how these oysters should be used. Thank you for helping us get this public health message out to food establishments that serve or sell this product.
If you have further questions, please contact your regulatory agency or an FDA Regional Retail Food Specialist.August 6, 2008
FDA Advice to Retail and Foodservice Operations on Raw Oysters Shipped With “For Cooking Only” Label As Part Of A Vibrio parahaemolyticus Control Plan
FDA is advising retail and foodservice operations to be aware that raw oysters shipped in containers bearing a“For Cooking Only” label may have a greater likelihood of containing harmful levels of the Vibrio parahaemolyticus (Vp) bacterium, which may cause illness, than do raw oysters not labeled in this manner.
Retail and foodservice operations should not purchase containers or packages of raw oysters that bear the “For Cooking Only” label unless the operator intends to fully cook the product before offering it for sale or service to the consumer.
The label is the result of new National Shellfish Sanitation Program provisions that call for oyster dealers to use the new label if harvesting conditions do not meet specific criteria for reduced risk of Vp contamination.
In addition to thoroughly cooking oysters that have the “For Cooking Only” label, food establishments that receive these oysters should take extra precaution to prevent cross-contamination of other foods and surfaces.
Molluscan shellfish, such as raw oysters, should be obtained only from sources listed on the Interstate Certified Shellfish Shippers List
We are providing the following information to you in advance of its delivery to the retail food trade organizations and asking your assistance in advising food establishments that raw oysters labeled “For Cooking Only” should not be sold or served to consumers in the raw form. FDA expects this “For Cooking Only” labeling as a control for the reduction of risk associated with Vibrio parahaemolyticus in oysters to be a temporary measure.
We are asking your assistance to help provide the attached information to retailers and restaurateurs who serve or sell raw oysters. If possible, please forward this advice to your organization’s members and to your state affiliate organizations as well. Certain states are requiring some shipments of oysters be labeled “For Cooking Only” as part of their Vibrio parahaemolyticus Control Plan under the National Shellfish Sanitation Program (NSSP).
This attachment explains what that means and how these oysters should be used. Thank you for helping us get this public health message out to food establishments that serve or sell this product.
If you have further questions, please contact your regulatory agency or an FDA Regional Retail Food Specialist.August 6, 2008
FDA Advice to Retail and Foodservice Operations on Raw Oysters Shipped With “For Cooking Only” Label As Part Of A Vibrio parahaemolyticus Control Plan
FDA is advising retail and foodservice operations to be aware that raw oysters shipped in containers bearing a“For Cooking Only” label may have a greater likelihood of containing harmful levels of the Vibrio parahaemolyticus (Vp) bacterium, which may cause illness, than do raw oysters not labeled in this manner.
Retail and foodservice operations should not purchase containers or packages of raw oysters that bear the “For Cooking Only” label unless the operator intends to fully cook the product before offering it for sale or service to the consumer.
The label is the result of new National Shellfish Sanitation Program provisions that call for oyster dealers to use the new label if harvesting conditions do not meet specific criteria for reduced risk of Vp contamination.
In addition to thoroughly cooking oysters that have the “For Cooking Only” label, food establishments that receive these oysters should take extra precaution to prevent cross-contamination of other foods and surfaces.
Molluscan shellfish, such as raw oysters, should be obtained only from sources listed on the Interstate Certified Shellfish Shippers List
Wednesday, August 6, 2008
Post Live Active Mixed Berry Crunch Cereal
August 5, 2008
ALMOND, PECAN, and WALNUT ALLERGY ALERT
Kraft Inadvertently Reships a Limited Number of Cases of
Previously Recalled Products
Arlington, VA -- Kraft Foods is recalling one code date of ?Post Live Active Mixed Berry Crunch Cereal? due to undeclared almonds, pecans, and/or walnuts.
The company is aggressively investigating the situation, and currently believes it received from the supplier a single tote of granola clusters for the Mixed Berry product with a small amount of nut-containing granola clusters inadvertently added.
This product was sold in stores nationwide.
The product comes in a 13-oz. box with a ?Best When Used By? date of 17DEC08 and UPC 00430000238900.
Tree nut allergic consumers are advised not to consume the product and are asked to call the Post Cereal Recall Line at 1-866-771-1511 for a full refund.
ALMOND, PECAN, and WALNUT ALLERGY ALERT
Kraft Inadvertently Reships a Limited Number of Cases of
Previously Recalled Products
Arlington, VA -- Kraft Foods is recalling one code date of ?Post Live Active Mixed Berry Crunch Cereal? due to undeclared almonds, pecans, and/or walnuts.
The company is aggressively investigating the situation, and currently believes it received from the supplier a single tote of granola clusters for the Mixed Berry product with a small amount of nut-containing granola clusters inadvertently added.
This product was sold in stores nationwide.
The product comes in a 13-oz. box with a ?Best When Used By? date of 17DEC08 and UPC 00430000238900.
Tree nut allergic consumers are advised not to consume the product and are asked to call the Post Cereal Recall Line at 1-866-771-1511 for a full refund.
Monday, August 4, 2008
Consumption of American Lobster
July 29, 2008
FDA Advises Against Consumption of American Lobster
(Maine Lobster) Tomalley Regulators find dangerous levels of toxins that cause Paralytic Shellfish Poisoning
The U.S. Food and Drug Administration today warned consumers to avoid eating tomalley in American Lobster (Maine Lobster), regardless of where the lobster was harvested, because of potential contamination with dangerous levels of the toxins that cause Paralytic Shellfish Poisoning (PSP).
American lobster, also known as Maine lobster, are harvested from the waters of the Atlantic Ocean from Northeastern Canada to South Carolina, inclusive.
The FDA advisory applies only to tomalley, the soft, green substance found in the body cavity of the lobster that functions as the liver and pancreas. Cooking does not eliminate the PSP toxins. However, studies have shown that, even when high levels of PSP toxins are present in lobster tomalley, lobster meat itself is typically unaffected.
Symptoms of PSP include tingling and/or numbness of the mouth, face or neck; muscle weakness; headache; and nausea. In extreme cases, when large amounts of the toxin are consumed, these symptoms can lead to respiratory failure and death. Symptoms usually occur within two hours of exposure to the toxin. Anyone experiencing these symptoms should seek medical attention.
PSP toxins normally occur from time to time in clams and other shellfish and are carefully monitored by state regulatory authorities. The FDA learned of this problem after routine sampling conducted by regulatory authorities in Maine and New Hampshire found dangerous levels of the toxins in lobster tomalley. Some shellfish beds have been closed in recent months due to elevated levels of PSP toxins.
Lobster tomalley normally does not contain dangerous levels of PSP toxins. The current high levels of PSP toxins likely are associated with an ongoing red tide episode in northern New England and eastern Canada. Authorities in Maine, Massachusetts and New Hampshire, as well as in Canada, have issued advisories cautioning against eating tomalley.
For more on seafood safety, please refer to http://www.cfsan.fda.gov/seafood1.html.
FDA Advises Against Consumption of American Lobster
(Maine Lobster) Tomalley Regulators find dangerous levels of toxins that cause Paralytic Shellfish Poisoning
The U.S. Food and Drug Administration today warned consumers to avoid eating tomalley in American Lobster (Maine Lobster), regardless of where the lobster was harvested, because of potential contamination with dangerous levels of the toxins that cause Paralytic Shellfish Poisoning (PSP).
American lobster, also known as Maine lobster, are harvested from the waters of the Atlantic Ocean from Northeastern Canada to South Carolina, inclusive.
The FDA advisory applies only to tomalley, the soft, green substance found in the body cavity of the lobster that functions as the liver and pancreas. Cooking does not eliminate the PSP toxins. However, studies have shown that, even when high levels of PSP toxins are present in lobster tomalley, lobster meat itself is typically unaffected.
Symptoms of PSP include tingling and/or numbness of the mouth, face or neck; muscle weakness; headache; and nausea. In extreme cases, when large amounts of the toxin are consumed, these symptoms can lead to respiratory failure and death. Symptoms usually occur within two hours of exposure to the toxin. Anyone experiencing these symptoms should seek medical attention.
PSP toxins normally occur from time to time in clams and other shellfish and are carefully monitored by state regulatory authorities. The FDA learned of this problem after routine sampling conducted by regulatory authorities in Maine and New Hampshire found dangerous levels of the toxins in lobster tomalley. Some shellfish beds have been closed in recent months due to elevated levels of PSP toxins.
Lobster tomalley normally does not contain dangerous levels of PSP toxins. The current high levels of PSP toxins likely are associated with an ongoing red tide episode in northern New England and eastern Canada. Authorities in Maine, Massachusetts and New Hampshire, as well as in Canada, have issued advisories cautioning against eating tomalley.
For more on seafood safety, please refer to http://www.cfsan.fda.gov/seafood1.html.
Vita Smoked Salmon
July 25th, 2008
To Whom It May Concern:
This letter is intended to inform you of a potential quality issue with a Vita Smoked Salmon product authorized for resale in your retail outlets. We have a conflicting test result for Lysteria, which means there is a potential health risk. To be on the safe side, we have decided to pull the product from your stores and warehouses. Details are below.
The product: 12/3oz. Vita Nova Salmon
UPC: 0 22635 70022 3
Code date: 11/16/08 198
Lot numbers (case codes) are as follows:
12 x 3oz Nat Nova Nov 16-08 01988A
12 x 3oz Nat Nova Nov 16-08 01988B
12 x 3oz Nat Nova Nov 16-08 01988C
Please hold all product currently at warehouse level for return to Vita Food Products, Inc.
Any product currently at store level should be pulled from shelves and placed on hold.
Thank you for your attention to this matter.
Sincerely,
Vita Food Products Inc.
2222 West Lake Street
Chicago, IL 60612
(312) 738-4500
www.vitafoodproducts.com
To Whom It May Concern:
This letter is intended to inform you of a potential quality issue with a Vita Smoked Salmon product authorized for resale in your retail outlets. We have a conflicting test result for Lysteria, which means there is a potential health risk. To be on the safe side, we have decided to pull the product from your stores and warehouses. Details are below.
The product: 12/3oz. Vita Nova Salmon
UPC: 0 22635 70022 3
Code date: 11/16/08 198
Lot numbers (case codes) are as follows:
12 x 3oz Nat Nova Nov 16-08 01988A
12 x 3oz Nat Nova Nov 16-08 01988B
12 x 3oz Nat Nova Nov 16-08 01988C
Please hold all product currently at warehouse level for return to Vita Food Products, Inc.
Any product currently at store level should be pulled from shelves and placed on hold.
Thank you for your attention to this matter.
Sincerely,
Vita Food Products Inc.
2222 West Lake Street
Chicago, IL 60612
(312) 738-4500
www.vitafoodproducts.com
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