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
Pharmedium Services, LLC is voluntarily recalling 2,232 bags of compounded Oxytocin injection because the drug was found to be subpotent.
Banner Pharmacy Services is recalling fentanyl citrate syringes because the agency could not ensure the product was sterile.
Banner Pharmacy Services is recalling 3,136 bags of Vancomycin 1.5 grams in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Banner Pharmacy Services is recalling 481 bags of Norepinephrine Bitartrate in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Pharmedium Services, LLC is voluntarily recalling 564 bags of compounded Oxytocin 10 units in Lactated Ringer's Injection because the drug was subpotent.
Banner Pharmacy Services is recalling 2,443 bags of Vancomycin in sodium chloride due to a lack of assurance of sterility.
Pharmedium Services, LLC is voluntarily recalling 24,486 bags of compounded Oxytocin 30 units in Lactated Ringer's because the drug was subpotent.
Banner Pharmacy Services is recalling 3,550 bags of Norepinephrine Bitartrate 8 mg in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Pharmedium Services, LLC is voluntarily recalling 60 bags of compounded Oxytocin injection because the drug was found to be subpotent.
Pharmedium Services, LLC is voluntarily recalling 1,152 bags of compounded Oxytocin 40 units in Lactated Ringer's USP because the drug was subpotent.
Pharmedium Services, LLC is voluntarily recalling 390 bags of compounded Oxytocin 20 units in Lactated Ringer's Injection due to subpotent drug levels.
Pharmedium Services, LLC is voluntarily recalling 978 bags of compounded Oxytocin in Lactated Ringer's Injection because the drug was subpotent.
The Harvard Drug Group is recalling Alprazolam Tablets, 0.25 mg, due to an out-of-specification result for an unknown impurity.
RXQ Compounding LLC is recalling 945 vials of methylprednisolone acetate injection because autoclave parameters were incorrect, raising concerns about product sterility.
Deserving Health International Corp is recalling Symbio Muc Eye eye drops because the product lacks assurance of sterility. The affected units were distributed throughout the United States.
United Pharmacy is recalling 268 vials of compounded Glutamine, Arginine, and Carnitine injection due to CGMP deviations and the absence of glutamine.
Inopak Ltd is recalling Option Systems and STYLE Antibacterial Hand Wash due to GMP deviations and potential bacterial contamination from a pump.
Pfizer is recalling 18,725 vials of Sterile Water for Injection due to cracked or chipped glass at the neck, which poses a non-sterility risk.
Genentech is recalling 16,882 units of Activase (alteplase) because the included sterile water vials may have cracked or chipped glass.
Pfizer is recalling 115,370 vials of Hydromorphone Hydrochloride Injection because a damaged sterilizing filter may have compromised sterility assurance during manufacturing.
Pfizer is recalling specific lots of Levophed (norepinephrine bitartrate) injection because a damaged sterilizing filter may have compromised sterility.
Amgen is recalling specific lots of Procrit (epoetin alfa) vials because glass flakes were found during routine quality inspection.
Chiavna Saffron LLC is recalling Super Panther 7K Capsules because FDA analysis found the product was tainted with sildendafil and tadalafil and marketed without an approved NDA/ANDA.
Leader Liquid Multivitamin Supplement for Infants and Toddlers is being voluntarily recalled due to possible contamination with B. cepacia, which can cause serious infections in vulnerable patients.
Bella Pharmaceuticals is recalling 200 prefilled BevaDex syringes nationwide because the company cannot guarantee the product's sterility.