We’ve rounded up a list of important US Food and Drug Administration and US Department of Agriculture recalls from this past week.
We’ve compiled a list of recalls issued by the US Food and Drug Administration (FDA) and US Department of Agriculture (USDA) from this past week:
Taylor Farms Illinois Inc. Issues Recall for Chicken Products due to Possible Processing Defect
Taylor Farms Inc., a Chicago, Ill. establishment, is recalling approximately 342 pounds of breaded chicken products due to a processing defect that may have led to undercooking of products, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The ready-to-eat breaded chicken items were produced August 3, 2019. The products subject to recall bear establishment number “EST. or P-21794” inside the USDA mark of inspection. These items were shipped to retail locations in Arkansas, Michigan, Mississippi, Ohio, Tennessee, and West Virginia where the products are sold in the deli section of retailers.
Read about the processing defect recall.
Tyson Foods, Inc. Issues Recall for Weaver Brand Chicken Products Due to Possible Contamination
Tyson Foods Inc., a Pine Bluff, Ark. establishment, is recalling approximately 39,078 pounds of Weaver brand frozen chicken patty product that may be contaminated with extraneous materials, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The frozen, fully cooked chicken items were produced on January 31, 2019. The products subject to recall bear establishment number “P-13456” printed on the back of the resealable plastic bag. These items were shipped to retail locations nationwide. The problem was discovered after the recalling firm notified FSIS of consumer complaints. Anyone concerned about an injury or illness should contact a healthcare provider.
Read about the possible contamination recall.
Dole Fresh Vegetables Issues Limited Recall of Baby Spinach Due to Salmonella Risk
Dole Fresh Vegetables, Inc. is voluntarily recalling a limited number of cases of baby spinach. The products being recalled are 6 oz Dole Baby Spinach bag, Lot code W20308A (UPC code 0-71430-00964-2), and 10 oz Dole Baby Spinach clamshell, Lot code W203010 (UPC code 0-71430-00016-8), both with Use-by dates of 08-05-2019, due to a possible health risk from Salmonella. Dole Fresh Vegetables is coordinating closely with regulatory officials. No illnesses have been reported in association with the recall.
The lot code and Use-by date are located on the upper right corner of the bag or on the top label of the clamshell; the UPC code is located on the bottom left corner of the back of the bag or on the bottom label of the clamshell. The impacted products were distributed in IL, IN, KY, MI, NJ, NY, OH, TN, VA, and WI. This product is expired and should no longer be on retail shelves. Consumers are advised to check product they have in their homes and discard any product matching these lot and UPC codes and Use-by dates.
Read about the baby spinach recall.
Pfizer Inc. Issues Voluntary Recall for 2 Lots of Relpax Due to Potential Contamination
Pfizer Inc. is voluntarily recalling RELPAX® (eletriptan hydrobromide) 40 mg tablets, lots AR5407 and CD4565, to the Patient level. Pfizer Inc. initiated this recall because these product lots may not meet Pfizer’s in-house microbiological specification for the potential presence of Genus Pseudomonas and Burkholderia.
Individuals who consume oral products contaminated with microorganisms are at risk of bacterial dissemination from the gut to the bloodstream potentially resulting in serious, life- threatening infections. In addition, there is risk of temporary gastrointestinal distress without serious infection. For the general population these risks are low; for certain vulnerable patient populations (such as patients with compromised immune systems, cystic fibrosis and chronic granulomatous disease) there may be the potential for serious adverse events including life- threatening infections. To date, Pfizer has not received any customer complaints or reports of adverse events related to this issue.
RELPAX®(eletriptan hydrobromide) is indicated for the acute treatment of migraine with or without aura in adults.
RELPAX ® (eletriptan hydrobromide) 40 mg tablets are packaged in cartons as indicated below. The affected lots were distributed nationwide to wholesalers, retailers, hospitals, and healthcare providers in the United States and Puerto Rico from June 2019, to July 2019.
Read about the relpax recall.
AWERS, Inc. Issues Salmon Caviar Recall Due to Clostridium Botulinum Contamination
AWERS, Inc. of Bellevue, WA is recalling Grained Salmon Caviar 95g (Sockeye Salmon Caviar) with “BEST BEFORE OCT 07 2020”, because it has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
Grained Salmon Caviar 95g was distributed in California, New York, Oregon, Washington and product may have further distributed to other states and Canada.
Product is packed in a metal tin with Cyrillic lettering. The tin is green, with red and white writing with an easy open pull lid. The “BEST BEFORE OCT 07 2020” is printed on the bottom on the tin.
No illnesses have been reported to date.
Read about the salmon caviar recall.
FDA Warns About Contamination of Texas Tripe Inc. Pet Food
The U.S. Food and Drug Administration is cautioning pet owners not to feed their pets any of the Texas Tripe brand raw frozen pet food listed below because several samples of Texas Tripe raw pet food have tested positive for Salmonella and/or L. mono.
The Office of the Texas State Chemist (OTSC) collected 23 finished product samples at Texas Tripe Inc. Of the 23 samples, 16 tested positive for L. mono and/or Salmonella.
FDA followed up these findings with an inspection and collected and analyzed samples of unopened finished product, after the firm performed corrective actions, from additional lots of some of the same products tested by OTSC. FDA testing showed some of the samples contained Salmonella and/or L. mono.
FDA and OSTC shared their test results with Texas Tripe Inc. The firm initiated a recall on July 3, 2019 by directly notifying some of its customers via email.
Salmonella and L. mono can affect both human and animal health. People with symptoms of Salmonella and L. mono infection should consult their health care providers. Consult a veterinarian if your pet has symptoms of Salmonella or L. mono infection.
Read about this pet food recall.