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
Liberty Drug & Surgical is recalling Methadone 10 mg/mL Injection vials because process deficiencies could have compromised sterility.
Liberty Drug & Surgical is recalling 6 vials of Methylcobalamin 1,000 mcg/mL Injectable due to process deficiencies that could 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.
Liberty Drug & Surgical is recalling 6 syringes of Cyanocobalamin 500 mcg/mL Injectable due to process deficiencies that could have compromised sterility.
Liberty Drug & Surgical is recalling 85 vials of 17-Hydroxyprogesterone injectable because process deficiencies may have compromised sterility.
Unichem Pharmaceuticals is recalling 4,776 bottles of hydrochlorothiazide 25 mg tablets because a pharmacist found a clopidogrel tablet in one bottle.
Mylan Institutional LLC is recalling 2,455 vials of Gemcitabine for Injection due to the presence of particulate matter.
Baxter Healthcare is recalling 189,120 bags of 0.9% Sodium Chloride Injection USP due to a customer complaint of an insect found inside a bag.
Mylan Institutional LLC is recalling specific lots of Gemcitabine for Injection due to the presence of particulate matter. The affected vials were distributed nationwide and in Puerto Rico.
Bausch & Lomb is recalling 13,995 bottles of Bromfenac Ophthalmic Solution, 0.09%, because preservative testing failed, raising concerns about sterility.
Mylan Institutional LLC is recalling Carboplatin Injection 450 mg/45 mL due to the presence of particulate matter.
GC Natural Nutrition is recalling PYROLA Advanced Joint Formula capsules because they contain undeclared prescription and over-the-counter drugs.
Baxter Healthcare is recalling 133,600 bags of 0.9% Sodium Chloride Injection USP due to the presence of an insect.
Mylan Institutional LLC is recalling 10,094 vials of Gemcitabine for Injection due to the presence of particulate matter.
Mylan Institutional LLC is recalling Methotrexate Injection vials due to the presence of particulate matter.
Baxter Healthcare is recalling 0.9% Sodium Chloride Injection USP due to complaints of particulate matter, leaks, and missing port protectors.
Mylan Institutional LLC is recalling 8,340 vials of Cytarabine Injection due to the presence of particulate matter. The affected product was distributed nationwide.
James G. Cole, Inc. is recalling all Maxam brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.
James G. Cole, Inc. is recalling all ASN brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.
Merck is recalling approximately 276,000 bottles of Temodar and Temozolomide capsules because cracked caps may fail to keep young children from accessing the medication.
The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 30/2/20 Injection in Oklahoma due to a lack of documentation proving proper environmental monitoring during production.
The Apothecary Shoppe is recalling specific lots of SIU-Papav/Phentol 30/1 mg/mL Injection due to a lack of documentation for environmental monitoring during production.
The Apothecary Shoppe LLC is recalling specific vials of Papaverine and Phentolamine Injection due to a lack of documentation confirming proper environmental monitoring during production.
The Apothecary Shoppe LLC is recalling SIU-Phent .4 mg/PGE1 20 mcg/mL Injection due to a lack of documentation for environmental monitoring during production.
The Apothecary Shoppe is recalling S-Methylcobalamin 1000 mcg/mL Injection because documentation for environmental monitoring during production was missing.