FDA Warning & Recall Information

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 […]

Chula Vista, California-based SoloVital.com has recalled all lots of its 30-caplet bottles of Umary Acido Hialuronica, Suplemento Alimenticio because the product has been found to contain two undeclared drug ingredients: diclofenac and omeprazole. The company announced the voluntary, consumer-level recall on July 15, 2024, after […]

According to the FDA, Bausch + Lomb/Synergetics Inc. has recalled four lots of its Bausch + Lomb I-Pack Injection Kit because officials are unable to verify the full sterilization of the products. Because of the risk of serious injury or death posed by the use […]

Wiers Farm, Inc., of Willard, Ohio, has announced a limited recall of whole cucumbers (under pack date June 5, 2024) and bagged salad cucumbers (under pack dates June 5 and 6, 2024) because the products may be contaminated with Listeria monocytogenes, reports the FDA. Consumers […]

According to the FDA, AB World Foods US, Inc. has recalled four production lots of its Al’Fez Natural Tahini in 5.6-ounce jars because of concerns that the products may contain the organism Salmonella. While healthy people infected with Salmonella typically experience short-term symptoms like fever, […]

The FDA is informing consumers of an Urgent Medical Device Recall announced by Baxter International Inc. regarding its Life2000 ventilators that come with an attached battery charger dongle. Initiated by the Deerfield, Illinois-based company on July 10, 2024, the recall is a response to reports […]

Reser’s Fine Foods, headquartered in Beaverton, Oregon, has recalled its 48-ounce (3-pound) containers of Hill Country Fare Mustard Potato Salad under “Use By” date “JUL/26/24” because the product may contain hard plastic foreign material, reports the FDA. Initiated by the company on July 2, 2024, […]

Abbott Medical has announced a Class I recall of its HeartMate LVAS System Monitor under all lots/serial numbers because a correction needs to be made to the Left Ventricular Assist System (LVAS) monitor, according to the FDA. Officials say affected units have screen issues that […]