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
Baptist Health Medical Towers Pharmacy is recalling 11 bags of Nafcillin 12 grams in 322 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 32 bags of Ceftriaxone 2 gram in 100 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 84 bags of Vancomycin 1250 mg in 250 mL 0.9% NS due to lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 21 Ascorbic Acid 500 mg syringes in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling two bags of Vancomycin IV solution in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling seven bags of Sodium Chloride 0.9% IV solution in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 18 syringes of 70% Ethanol-lock Solution in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 14 bags of IV piperacillin-tazobactam in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling Ceftriaxone IV bags in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 53 bags of IV piperacillin-tazobactam in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling Vancomycin IV bags in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling four bags of Piperacillin-Tazobactam in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling three Deferoxamine cassettes in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 16 bags of Ceftriaxone 2 gram IV solution in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy recalls Remicade IV bags in Arkansas due to lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling ertapenem IV bags in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 0.9% Sodium Chloride IV bags in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling Milrinone IV bags in Arkansas due to a lack of sterility assurance.
Taro Pharmaceuticals is recalling 62,800 tubes of Topicort cream because the medication contained less active ingredient than labeled.
Lupin Pharmaceuticals is recalling 570 vials of Ceftriaxone for Injection USP, 2 g, because the active pharmaceutical ingredients used in manufacturing failed specifications.
Lupin Pharmaceuticals is recalling Ceftriaxone for Injection vials because they were manufactured using active pharmaceutical ingredients that failed specifications.
Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP, 500 mg, because the active ingredients used in manufacturing failed specifications.
Lupin Pharmaceuticals is recalling specific lots of Ceftriaxone for Injection USP because they were manufactured using active pharmaceutical ingredients that failed specifications.
Lupin Pharmaceuticals Inc. is recalling Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient because intermediates failed specifications.
Master Herbs is recalling Licorice Coughing Liquid because it contains undeclared morphine and was marketed without an approved NDA or ANDA.