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
Medline is recalling sterile incision and drainage trays because the povidone-iodine prep pads contain less iodine than labeled.
Medline Industries is recalling sterile staple remover trays containing subpotent povidone-iodine prep pads. The iodine concentration is below the labeled claim of 0.85%.
A&H Focal Inc. is recalling Yanshijiaonang capsules because FDA analysis found they contain sildenafil, an unapproved drug for which safety and efficacy have not been established.
Medline Industries is recalling Debridement Trays because the iodine concentration in the prep pads is below the label claim.
A&H Focal Inc. is recalling DADIYONGSHI XIANGGANGTIANLONGSHENGWU tablets because they contain sildenafil, an unapproved drug for erectile dysfunction.
A&H Focal Inc. is recalling Germany Niubian tablets because FDA analysis found they contain sildenafil, an unapproved drug for which safety and efficacy have not been established.
The FDA is recalling ZHANSHENG WEIGE CHAOYUE XILISHI tablets because they contain sildenafil, an unapproved drug for which safety and efficacy have not been established.
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.
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 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.
Sun Pharmaceutical Industries is recalling 393 vials of Doxorubicin Hydrochloride Liposome Injection due to a lack of assurance of sterility.
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 Major Poly-Vita Drops w/ Iron due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Rugby Calcionate Syrup 16 oz. 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.
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 D3 Vitamin liquid 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 Liquid Vitamin C Supplement 500 mg due to the presence of yeast and potential contamination with B. cepacia.
Pharmatech LLC is recalling Rugby Polyvitamin Liquid in Michigan due to the presence of yeast and potential contamination with B. cepacia.
DLC Laboratories is recalling Earth's Care Eczema Lotion due to microbial contamination. The product was distributed nationwide.
Pharmatech LLC is recalling Major Ferrous Drop Iron Supplement due to the presence of yeast and potential contamination with B. cepacia.