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
Baxter Healthcare is recalling 54,528 bags of 5% Dextrose Injection because the bags may leak, compromising sterility.
SCA Pharmaceuticals is recalling 221 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The product was distributed in LA, PA, NY, and WI.
Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride bags because the company cannot assure the product's sterility.
Phillips Co. is recalling Diabecline brand Topical Ointment First Aid Antibiotic because FDA inspections found significant manufacturing deviations that question the product's safety and quality.
Alvogen, Inc. is recalling 5,100 vials of Clindamycin Injection USP due to a lack of assurance of sterility. The affected product was distributed nationwide.
Phillips Co. is recalling Tetracycline-ABC Brand Topical Ointment because FDA inspections found significant manufacturing deviations that raise questions about product safety and quality.
Phillips Co. is recalling VenomX Zinc Acetate Skin Protectant because FDA inspections found manufacturing practices that question the product's safety and quality.
Alvogen, Inc. is recalling specific lots of Clindamycin Injection USP due to a lack of assurance of sterility. The recall covers 71,825 vials distributed nationwide.
Alvogen, Inc. is recalling 72,575 vials of Clindamycin Injection USP due to a lack of assurance of sterility. The affected lots were distributed nationwide.
Phillips Co. is recalling StingMed Insect Bites Skin Protectant because FDA inspections found significant manufacturing deviations that raise questions about the product's safety and quality.
Phillips Co. is recalling TetraStem Topical Ointment First Aid Antibiotic because FDA inspections found significant manufacturing deviations that raise questions about product safety and quality.
Fagron Compounding Services is voluntarily recalling 1,056 syringes of Succinylcholine Chloride because the company cannot ensure the product is sterile.
Phillips Co. is recalling StaphWash+Plus+ Skin Protectant because FDA inspections found manufacturing practices that question the product's safety and quality.
Allergan is recalling 648 units of Blephamide ophthalmic ointment because stability testing showed impurities exceeding specifications.
Vi-Jon, Inc. is recalling 52,212 bottles of Magnesium Citrate Saline Laxative because glass particles were found in the product.
Complete Pharmacy and Medical Solutions LLC is recalling 1,890 syringes of Human Chorionic Gonadotropin (HCG) due to confirmed mold contamination.
Complete Pharmacy and Medical Solutions LLC is recalling 49 vials of Human Chorionic Gonadotropin due to confirmed bacterial contamination.
Safecor Health LLC is recalling 856 bottles of Doxycycline 100mg tablets in Massachusetts and New York due to Current Good Manufacturing Practice (CGMP) deviations.
Bausch & Lomb is recalling specific lots of NasalCrom nasal spray due to potential microbial contamination in the manufacturing water.
Qualgen is recalling Estradiol 12.5 mg pellets due to CGMP deviations and a lack of quality assurance. The recall covers 4,883 pellets distributed nationwide.
Spectrum Laboratory Products is recalling levonorgestrel active pharmaceutical ingredient due to manufacturing deviations found by the FDA.
MedPark Pharmacy is recalling methylcobalamin 1mg/1mL injection vials because the company cannot ensure the product is sterile. The affected lot was distributed to a patient in Maryland.
Qualgen is recalling Estradiol 22 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 1,666 pellets distributed nationwide.
SCA Pharmaceuticals is recalling fentanyl citrate injectable bags because they are leaking at the seam, which compromises sterility.
SCA Pharmaceuticals is recalling 118 bags of fentanyl injection due to seam leaks that compromise sterility. The product was distributed nationwide in the USA.