Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Amgen is recalling 11,434 vials of Kyprolis (carfilzomib) injection because potential cracks in the glass vials may compromise sterility.
Woodland Foods is recalling D'Allesandro Salt-Free Roasted Sunflower Seeds due to potential Listeria contamination. The product was distributed to food distributors in 26 states.
Making It a Lifestyle is recalling 3rd Degree capsules because they contain undeclared sibutramine and were marketed without an approved NDA or ANDA.
Virtus Pharmaceuticals is recalling Hyoscyamine Sulfate tablets because they failed content uniformity specifications, resulting in both superpotent and subpotent doses.
Colonia Care Pharmacy is recalling C-PAV/PHENTOL/PGE1 injectable drug products due to lack of assurance of sterility. The recall affects products distributed in New Jersey and New York.
Interbake Foods is recalling Girl Scout Peanut Butter Sandwiches because a single lot of peanut butter used contained elevated aflatoxin levels.
Wakefern Food Corp. is recalling Gourmet Chocolate Dipped Cookies because they may contain metal pieces. The product was distributed in six states.
Chaos and Pain is recalling its Cannibal Ferox Amped pre-workout supplement because it contains an undeclared prohibited substance.
Naturecom is recalling 500g bags of DMAA powder because the product may contain 1,3-dimethylamylamine. The recall covers products distributed nationwide and internationally.
Coliman Pacific Corp is recalling jalapeno peppers because they may be contaminated with Salmonella. The affected product was distributed in California and Arizona.
The FDA is recalling Ultroid Hemorrhoid Management Systems because they were not manufactured under required quality system controls.
Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe because they may be contaminated with Listeria monocytogenes.
Wakefern Food Corp. is recalling 24-count sugar cookies due to the potential presence of metal pieces. The product was distributed in six states.
Amendia, Inc. is recalling 96 units of Black Widow 6.6mm spinal screws due to a design defect in the mating feature between the plate and screw.
Baxter Healthcare is recalling 30,910 bags of Fluconazole Injection due to confirmed customer complaints of leaking bags, which compromises sterility.
Midwest International Corp is recalling Heihujiaoyupai canned fish because it is a low acid canned food without a registered manufacturer and scheduled process.
Samuel Adams Brewery is recalling Apple Orchard Crisp Apple Hard Cider because bottles may burst due to re-fermentation.
Medtronic is recalling 1,293,169 Clearify Visualization Systems because a breach of the sterile barrier compromises product sterility.
Wakefern Food Corp. is recalling 24-count Take&Bake Sugar Cookies because they may contain metal pieces. The product was distributed in six states.
Merge Healthcare is recalling OrthoCase software because measurements change after saving, potentially causing patient injury or delayed diagnosis.
Novo Nordisk is recalling 71,215 GlucaGen HypoKits because the syringe needles may be detached. The recall covers lots expiring in September 2017.
Virtus Pharmaceuticals is recalling Hyoscyamine Sulfate sublingual tablets because they failed content uniformity specifications, resulting in tablets that are either superpotent or subpotent.
Colonia Care Pharmacy is recalling C-PAV/PHENTOL/ATROP/PGE1 injectable products due to lack of assurance of sterility. The recall affects products distributed in New Jersey and New York.
Wakefern Food Corp. is recalling Dipped Chocolate Chip Cookies because they may contain metal pieces. The product was distributed in six states.
Wakefern Food Corp. is recalling 24-count peanut butter cookies due to the potential presence of metal pieces.