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 deaths or serious injuries are reported, 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
Dr. Reddy's Laboratories is recalling Atorvastatin Calcium 10 mg tablets because stability testing showed out-of-specification results for total degradation impurities.
Dr. Reddy's Laboratories is recalling Atorvastatin Calcium 20 mg tablets because stability testing revealed out-of-specification total degradation impurities.
The FDA is recalling Hard Times For Men capsules because they contain undeclared sildenafil and were marketed without an approved NDA or ANDA.
BotanicalNow is recalling BodySlim Herbal capsules because FDA analysis found undeclared sibutramine, a substance not approved for use in this product.
Sun Pharmaceutical Industries is recalling 393 vials of Doxorubicin Hydrochloride Liposome Injection due to a lack of assurance of sterility.
Pharmatech LLC is recalling Rugby D3 Vitamin liquid due to the presence of yeast and potential contamination with B. cepacia.
International Laboratories, Inc. is recalling Pravastatin Sodium Tablets, 20 mg, because bottles may contain 10 mg tablets. Patients should contact their healthcare provider.
Advanced Pharma Inc. is recalling 25 bags of Magnesium Sulfate IV solution in Texas due to subpotent product.
Pharmatech LLC is recalling Rugby Polyvitamin Liquid in Michigan due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Rugby Tri-Vitamin Liquid due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Major Tri-Vita Drops due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Rugby Cerovite Liquid 236 mL due to the presence of yeast and potential contamination with B. cepacia. The recall covers all lots remaining within expiry in Michigan.
Pharmatech LLC is recalling Rugby Calcionate Syrup 16 oz. due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Rugby Liquid Vitamin C Supplement 500 mg due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Rugby Ferrous Sulfate Elixir 473 mL due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Rugby Poly-Vitamin w/ Iron Liquid 50 mL due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Major Poly-Vita Drops w/ Iron due to the presence of yeast and potential contamination with B. cepacia.
International Laboratories, Inc. is recalling Pravastatin Sodium Tablets 10 mg because bottles may contain 20 mg tablets.
DLC Laboratories is recalling Earth's Care Eczema Lotion due to microbial contamination. The product was distributed nationwide.
Pharmatech LLC is recalling Rugby FER Iron Liquid 50 mL due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Major Ferrous Drop Iron Supplement due to the presence of yeast and potential contamination with B. cepacia.
Odan Laboratories is recalling 179 kits of Dry to Normal Skin Starter Kit because the product failed stability specifications at 12 months.
Odan Laboratories is recalling 21 jars of Day Cream SPF15 because the product failed stability specifications at 12 months.
Marksans Pharma Inc. is recalling ibuprofen tablets due to odor complaints linked to Current Good Manufacturing Practice (CGMP) deficiencies.
Marksans Pharma Inc. is recalling 4,127,500 ibuprofen tablets due to odor complaints and CGMP deficiencies. The product was distributed nationwide to repackaging firms.