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
Spartan Chemical Co Inc is voluntarily recalling 1,200 cases of Lite'n Foamy Eucalyptus Mint Sanitizing Handwash due to Current Good Manufacturing Practice (CGMP) deviations.
Novo Nordisk is recalling OZEMPIC sample pens stored below 32°F, which may cause lack of efficacy and damage to the cartridge and pen-injectors.
Spartan Chemical Company is voluntarily recalling 26,328 cartridges of foamyiQ Lemon Blossom Hand Sanitizer due to Current Good Manufacturing Practice (CGMP) deviations.
Macleods Pharma USA is recalling Candesartan Cilexetil tablets because they failed impurity and degradation specifications.
Spartan Chemical Co Inc is voluntarily recalling 960 containers of Lite'n Foamy Healthcare Personnel Handwash due to CGMP deviations. The product was distributed nationwide in the US, Puerto Rico, and Mexico.
Enovachem Pharmaceuticals is recalling Methylprednisolone Tablets due to misaligned printing on the blister card that renders dosing instructions illegible.
Teligent Pharma is recalling Lidocaine Ointment USP, 5%, due to failed viscosity specifications. The recall covers 62,040 tubes distributed nationwide.
Sun Pharmaceutical Industries is recalling 91,211 syringes of Ganirelix Acetate Injection because the product failed impurities and degradation specifications.
Alembic Pharmaceuticals is recalling 12,288 bottles of Telmisartan 20 mg tablets due to a label mixup. The product was distributed nationwide in the United States.
Kimberly-Clark is recalling Scott Moisturizing Foam Hand Sanitizer because some bottles containing Foam Skin Cleanser soap are incorrectly labeled as hand sanitizer.
X-Gen Pharmaceuticals is recalling Neomycin Sulfate Tablets 500mg because a microbiological assay failed to meet stability specifications.
Apotex Corp. is recalling Guanfacine Extended-Release tablets because they contain trace amounts of Quetiapine Fumarate.
Cosette Pharmaceuticals is recalling specific lots of Mometasone Furoate Topical Solution due to Current Good Manufacturing Practice (CGMP) deviations.
Washington Homeopathic Products, Inc. is recalling LCL-2-0191 because it was manufactured with Potassium Chloride instead of Potassium Phosphate.
Sun Pharmaceutical Industries is recalling 2,520 bottles of Metformin Hydrochloride Extended-Release Tablets due to failed moisture limits.
Washington Homeopathic Products, Inc. is recalling Macula Pellets Homeopathic Medicine because the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Washington Homeopathic Products, Inc. is recalling 114 bottles of Sp-4 solution because the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Zydus Pharmaceuticals is recalling Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.
Zydus Pharmaceuticals is recalling 1,638 packs of Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.
Cardinal Health Inc. is voluntarily recalling 48 boxes of Tremfya (guselkumab) Injection due to temperature abuse. The affected product was distributed to Alabama, Louisiana, Mississippi, and Tennessee.
Adam's Secret Extra Strength 1500 is being recalled because FDA analysis found unapproved drugs tadalafil and sildenafil in the product.
The FDA is recalling Adam's Secret Extra Strength 3000 because it contains unapproved drugs tadalafil and sildenafil.
Golden State Medical Supply is recalling Omeprazole Delayed Release Capsules because stability testing revealed unknown impurities.
ICU Medical is recalling 425,628 bottles of 0.9% Sodium Chloride Irrigation due to the presence of particulate matter.
Sagent Pharmaceuticals is recalling specific lots of Phenylephrine Hydrochloride Injection due to customer complaints of loose vial overseals that may compromise sterility.