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
South Coast Specialty Compounding is recalling Chorionic Gonadotropin/Hydroxocobalamin Injectable vials due to potential penicillin cross-contamination.
South Coast Specialty Compounding is recalling 24 prescriptions of Estradiol cream due to potential penicillin cross contamination.
South Coast Specialty Compounding is recalling Bi-Est Testosterone cream due to potential penicillin cross-contamination. The affected products were distributed nationwide.
South Coast Specialty Compounding is recalling 172 vials of Artesunate Lyophilized Powder for Injection due to potential penicillin cross-contamination.
Vintage Pharmaceuticals is recalling 8,705 bottles of Lisinopril 40 mg tablets because they failed dissolution specifications. The affected lots were distributed nationwide and in Puerto Rico.
Silarx Pharmaceuticals is recalling 576 bottles of Lamivudine Oral Solution because the expiration date on the carton does not match the bottle label.
Qualitest Pharmaceuticals is recalling 21,552 bottles of 300 mg Allopurinol tablets because some tablets are oversized and discolored.
Teva Pharmaceuticals USA is recalling ADRUCIL (fluorouracil injection) vials due to the presence of silicone rubber and fluorouracil crystals in the solution.
PharMEDium Services, LLC is recalling 240 bags of Heparin Sodium Injection USP 25,000 Units in 250 mL bags due to the presence of particulate matter.
PharMEDium Services, LLC is recalling 48 bags of Epinephrine HCl injection due to the presence of particulate matter in the solution.
PharMEDium Services, LLC is recalling 264 bags of Epinephrine HCl injection due to the presence of particulate matter in the saline solution.
PharMEDium Services is recalling 36 bags of Epinephrine HCl injection due to the presence of particulate matter in the solution.
Liberty Drug & Surgical is recalling 2 vials of Papaverine/Phentolamine/PGE-1 Injectable because process deficiencies may have compromised sterility.
Reckitt Benckiser is recalling Mucinex Fast-Max Cold & Sinus liquid because the back of the bottle is missing active ingredients and safety warnings.
Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.
Liberty Drug & Surgical is recalling 22 vials of Dexamethasone 24 mg/mL Injectable due to process deficiencies that could have compromised sterility.
Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.
Liberty Drug & Surgical is recalling 85 vials of 17-Hydroxyprogesterone injectable because process deficiencies may have compromised sterility.
Liberty Drug & Surgical is recalling Lidocaine/Sodium Chloride injectable vials because process deficiencies may have compromised sterility.
Reckitt Benckiser is recalling Mucinex Fast Max Night Time Cold & Flu liquid bottles because the back label is missing active ingredients and safety warnings.
Liberty Drug & Surgical is recalling Papervine/Phentolamine/PGE-1 Injectable vials because process deficiencies may have compromised sterility.
Liberty Drug & Surgical is recalling Papaverine/Phentolamine/PGE-1 Injectable vials because process deficiencies could have compromised the product's sterility.
Reckitt Benckiser is recalling Mucinex Fast Max liquid bottles where the back label is missing active ingredients and safety warnings.
Liberty Drug & Surgical is recalling Glycerin 72% Injection vials because process deficiencies may have compromised sterility. The product was distributed to physicians and facilities in NJ and NY.
GlaxoSmithKline is recalling Bactroban Cream (mupirocin calcium) 2% because the product was contaminated with penicillin and foreign substances during manufacturing.