FDA Warning & Recall Information

Brooklyn, New York-based AMB Food Inc. has recalled its 8-ounce bags of Pop a Nosh Mixed Munch Regular and Honey BBQ snacks because the products contain wheat, a major allergen not disclosed on an ingredient panel. Individuals who live with a severe sensitivity or allergy […]

Sagent Pharmaceuticals, of Schaumburg, Illinois, has voluntarily recalled two lots of Docetaxel Injection, USP, in 80 mg per 8 mL multi-dose vials as well as in 160 mg per 16 mL multi-dose vials, because particulate matter may be found in the stopper of the product. […]

A May 6, 2024 press release informing the public of Palmer Candy Company’s recall of white confectionary products has since been updated to include two more items, as well as additional best-by dates of six products previously included, according to the FDA. The recall, which […]

According to the FDA, Vyaire Medical, Inc.’s April 8, 2024, recall of its Twin Tube has been identified as Class I, the most serious type, because use of the product could lead to major injuries or death. The recall, which was updated on May 23, […]

According to the FDA, Mars Petcare US, of Franklin, Tennessee, has recalled 315 44-pound bags of Pedigree® Adult Complete Nutrition Grilled Steak & Vegetable Flavor Dry Dog Food because the bag may contain loose pieces of metal. Officials noted that only products in the above […]

On May 22, 2024, the FDA released a communication warning consumers that Hologic, Inc.’s recall of its BioZorb Marker has been identified as Class I, the most serious type, because use of the product may lead to major injuries or death. Initiated by Hologic, Inc., […]

United Supermarkets, of Lubbock, Texas, is warning consumers in Texas and New Mexico that white coated confectionary items have been voluntarily recalled by its supplier Palmer Candy because the products may be contaminated with Salmonella. Palmer Candy’s own liquid coating supplier alerted the company that […]

According to the FDA, Draeger, Inc.’s March 10, 2024, recall of its Perseus A500 Anesthesia System has been identified as identified as Class I, the most serious type, because officials have determined that use of the devices put patients at risk for major injuries or […]

According to the FDA, Aldi Deli Macaroni Salad, 32 oz, under use-by date June 3, 2024, has been recalled by Reser’s Fine Foods because of incorrect labeling, which fails to declare wheat as an allergen in the product. Initiated by the Beaverton, Oregon-based company on […]

According to the FDA, Route 92 Medical Inc. has recalled three lots of its Tenzing 7 Delivery Catheter products after receiving multiple reports of “distal tip separation at the proximal marker band.” Initiated by the firm on March 8, 2024, an FDA update posted May […]

According to the FDA, Great Value Organic Black Chia Seeds, in 32-ounce packages, has been voluntarily recalled by Natural Sourcing International because some of the products may be contaminated with the organism Salmonella. Although healthy people with a Salmonella infection typically experience short-lived symptoms like […]

The U.S. Food and Drug Administration issued an alert Tuesday warning patients, caregivers, and health care providers about potential cross-compatibility issues with autoinjector devices used to administer glatiramer acetate injection for treating multiple sclerosis. According to the FDA, using an autoinjector that is incompatible with […]