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
Irwin Naturals is recalling Dual Action Cleanse and Daily Digestive Enzymes because they may be contaminated with chloramphenicol.
Mylan Pharmaceuticals is recalling 521 bottles of Ciprofloxacin 250 mg tablets because they were not manufactured according to Good Manufacturing Practices.
American Laboratories Inc is recalling specific lots of enzyme blend powder due to potential contamination with Chloramphenicol.
GE Pharma LLC is recalling 480 units of Creafuse Grape, 600 Grams, because the product contains 1,3 dimethylamylamine (DMAA).
American Laboratories Inc is recalling PC Blend 14 enzyme powder due to potential contamination with Chloramphenicol. The product was distributed to specific states.
Kashmir Crown Baking LLC is recalling Pista Khatie cookies because testing found undeclared egg allergen, despite the label stating the product contains no eggs.
American Laboratories Inc is recalling Xylanase 150,000XU enzyme powder because it may be contaminated with Chloramphenicol. The product was distributed to five states.
Mylan Pharmaceuticals is recalling specific lots of Amlodipine Besylate and Benazepril HCl capsules because they were not manufactured according to Good Manufacturing Practices.
Safeway is recalling Angel Food Cake Loaves because the labels failed to list milk and soy as ingredients.
Mylan Pharmaceuticals is recalling Amlodipine Besylate Tablets 10 mg because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.
GE Pharma LLC is recalling Creafuse Fruit Punch, 600 Grams, because the product contains 1,3 dimethylamylamine (DMAA).
Mylan Pharmaceuticals is recalling Amlodipine Besylate Tablets, 5 mg, because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.
Giant Eagle is recalling Candy Place Candy Corn Mix because it contains undeclared milk, egg, peanut, and soy allergens.
Mylan Pharmaceuticals is recalling Ciprofloxacin 500 mg tablets because they were not manufactured according to Good Manufacturing Practices.
American Laboratories Inc is recalling Xylanase enzyme powder samples due to potential contamination with Chloramphenicol. The affected lots were distributed to five states.
Mylan Pharmaceuticals is recalling specific lots of Amlodipine Besylate and Benazepril HCl capsules because they were not manufactured according to Good Manufacturing Practices.
Sandoz is recalling specific lots of Ropinirole Extended-Release Tablets 2 mg due to potential cross-contamination with mycophenolate mofetil.
American Laboratories Inc is recalling Pectinase 3,500 ENDO-PG/G enzyme powder due to potential chloramphenicol contamination. The product was distributed to Iowa, Utah, Nevada, Nebraska, and California.
Smiths Medical ASD, Inc. is recalling Portex Spinal Anaesthesia Trays because visual particulate was found in the glass ampules of 5% Lidocaine HCL and 7.5% Dextrose Injection.
American Laboratories Inc is recalling Ultra Blend 102 enzyme powder due to potential Chloramphenicol contamination. The product was distributed to five states.
Mylan Pharmaceuticals is recalling Amlodipine Besylate and Benazepril HCl capsules because they were not manufactured according to Good Manufacturing Practices.
Safeway is recalling Holiday Decorated Angel Food Cakes because the labels failed to list milk and soy as ingredients.
Mylan Pharmaceuticals is recalling 28,140 bottles of 200 mg Lamotrigine tablets because they were not manufactured according to Good Manufacturing Practices.
Amgen is recalling 4,163 Prolia (denosumab) prefilled syringes because visible cellulose fibers were found during routine quality checks.
West-Ward Pharmaceutical Corp. is recalling Irinotecan Hydrochloride Injection because an incorrect calculation resulted in an assay higher than the labeled claim.