FDA Warning & Recall Information

According to the FDA, Ozone Park, New York-based American Spices, LLC, has recalled its Spice Class brand Ground Cinnamon after an analysis performed by New York State Department of Agriculture and Markets (NYSAGM) showed the product to contain high than acceptable levels of lead. The […]

The FDA is informing consumers that four devices are included in Megadyne Medical Product, Inc.’s recall of Mega Soft Universal Patient Return Electrodes because the Instructions for Use and product labeling need to be updated to restrict device use to patients aged 12 and older. […]

According to the FDA, as many as 19 different packaged vegetable products have been recalled by Supreme Service Solutions LLC because of a potential Listeria monocytogenes contamination. Announced by the company on July 26, 2024, the action concerns Supreme Produce-branded items that originated from Weirs […]

The FDA is advising consumers that Hikma Pharmaceuticals PLC (Hikma, Group) has extended its retail-level and single-lot recall of Acetaminophen Injection, 1000mg/100mL (10mg/mL) to the consumer level, per an update on the agency’s website on July 22, 2024. The company had voluntarily recalled all products […]

Van Leeweun Ice Cream, headquartered in Brooklyn, New York, has recalled pints of its Vegan Pumpkin Cinnamon Roll under lot number 24V094 because the finished product may contain peanuts, an allergen not declared on its ingredient panel, reports the FDA. Individuals who live with a […]

Batavia, Illinois-based Aldi Inc., in collaboration with Wiers Farm, Inc. and R.S. Hanline Co Inc., has recalled Freshire Farms jalapeños, green peppers, and green beans because the organism Listeria monocytogenes may be present on the products, reports the FDA. In healthy individuals, a Listeria infection […]

According to the FDA, Bronx, New York-based ALB-USA Enterprises, Inc. has recalled its ALB Flavor-branded Cinnamon Powder after an analysis by the Connecticut Agriculture Experiment Station (CAES) indicated that the product may contain above-normal levels of lead. Consumers should be aware that those who are […]

Austin, Kentucky-based Kenny’s Farmhouse Cheese has recalled batch 231129 of its St. Jerome cheese after routine testing conducted by the Kentucky Department of Public Health showed the organism Listeria monocytogenes to be present in a single package, reports the FDA. While healthy people infected with […]

East Windsor, New Jersey-based Aurobindo Pharma USA, Inc. has recalled a single lot of Healthy Living Migraine Relief, Acetaminophen 250mg, Aspirin (NSAID) 250mg & Caffeine 65mg tablets on behalf of AuroHealth because the product does not have a manufacturer label, reports the FDA. The voluntary, […]

Indio, California-based Stutz Packing Company has recalled its 1-pound bags of shelled walnuts because a potential Listeria monocytogenes contamination has been identified in the product, reports the FDA. While healthy people infected with the organism may only experience short-lived symptoms like “high fever, severe headache, […]

According to the FDA, Baxter International Inc., of Deerfield, Illinois, has recalled certain lots of its Volara system single-patient use circuit and blue ventilator adapter assembly because of a potential device defect. The company says it received reports of the product’s handset plug disconnecting from […]

According to the FDA, Malvern, Pennsylvania-based Endo, Inc announced that a single lot of Clonazepam Orally Disintegrating Tablets, USP (C-IV) 0.25 mg tablets has been recalled by one of its subsidiaries, Endo USA, Inc., because the product carton may feature the incorrect strength. Officials say […]