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
Western Drug is recalling 68 containers of Tri-Mix ED Injection because the product lacks assurance of sterility. The recall covers distribution in eight U.S. states.
Western Drug is recalling 15 containers of Quad Mix Inj because the company cannot ensure the product is sterile.
Western Drug is recalling Sodium Chloride 0.9% Injections because the agency could not ensure the product was sterile. The recall covers all lots distributed nationwide.
Western Drug is recalling Heparin 1000 Unit/mL Injection because the product lacks assurance of sterility. The recall covers two containers distributed nationwide.
Western Drug is recalling Squaric Acid 4% Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Magnesium Chloride Injection because the product lacks assurance of sterility. The recall covers two containers distributed nationwide.
Western Drug is recalling Calcium EDTA 300mg/mL Injection because the product lacks assurance of sterility. The recall affects two containers distributed nationwide.
Life Science Pharmacy Inc. is recalling Hydroxocobalamin Injection due to potential penicillin cross-contamination. The recall covers all lot numbers and expiration dates distributed nationwide.
Western Drug is recalling AMP50/B121MG Complex Mix/ML Injection because the product lacks assurance of sterility. The recall covers four containers distributed nationwide.
Life Science Pharmacy Inc. is recalling E3 Cream compounded in Harriman, NY, due to potential penicillin cross-contamination.
Western Drug Inc. is recalling four containers of Sodium Bicarbonate 8.4% Injection due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Western Drug is recalling Lidocaine Injection 1% and 2% due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Life Science Pharmacy Inc. is recalling BI-EST Gels because they may be contaminated with penicillin. The recall covers all lots distributed nationwide.
Western Drug is recalling Heparin Sodium 30,000U/30ML Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling 36 containers of Tri-Amino OAC 1:1:1 300mg/mL because the product lacks assurance of sterility.
Western Drug is recalling four containers of Dexpanthanol B5 250mg/mL Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Phenylephrine 500mcg/mL Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling M-Cobalamin 2/Folate 5mg/mL Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Lipodissolve 100/50mg Injection Solution because the company cannot assure the product is sterile.
Western Drug is recalling two containers of Butor/Nal/Hydro Nasal Suspension because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling two containers of Tacrolimus 0.02% Opth Sol due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Western Drug is recalling Gent 80 mg/Liter Nasal spray because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling M-Cobalamin (B12) injections because the FDA determined there is a lack of assurance of sterility. The recall affects 3 containers distributed nationwide.
Western Drug is recalling Prostin Injection due to a lack of assurance of sterility. The recall covers 16 containers distributed nationwide.
Western Drug is recalling 46 containers of Methylcobalamin Injection because there is a lack of assurance of sterility.