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
Genzyme Corporation is recalling 24 vials of Lumizyme (alglucosidase alpha) because the packaging may have incorrect or missing lot and expiration dates.
Praxair Inc. is recalling 382 cylinders of medical air nationwide after a customer reported an odor when turning on a cylinder.
Pfizer is recalling 63,636 bottles of Robitussin Peak Cold Liquid nationwide due to a label mix-up. Consumers should stop using the product and return it to the point of purchase.
Sagent Pharmaceuticals is recalling specific lots of Fluconazole Injection due to cross-contamination with metronidazole. The affected product is distributed nationwide and in Puerto Rico.
AGA Gas Inc is recalling 1,500 gallons of bulk liquid oxygen because the delivery trailer may not have met GMP requirements prior to filling.
AstraZeneca is recalling Tudorza Pressair inhalers because some units have actuation counters set to a number other than 60.
Teva Pharmaceuticals is recalling Paricalcitol Capsules because stability testing revealed out-of-specification impurities. The recall covers 30,891 bottles distributed nationwide and in Puerto Rico.
Pharmedium Services, LLC is recalling 6,816 bags of subpotent epinephrine injection due to discoloration and FDA-confirmed potency issues.
Medical Park Homecare is recalling compressed oxygen cylinders filled using out-of-date gauges. The recall involves M6, D, and E tanks distributed in Oklahoma.
Teva Pharmaceuticals USA is recalling 576 bottles of Nabumetone 750 mg tablets because they lack required leaflets and approved labels.
Pharmedium Services, LLC is recalling specific lots of repinephrine bitartrate injection bags due to subpotency and discoloration confirmed by FDA analysis.
Virtus Pharmaceuticals is recalling Virt-Nate Prenatal/Postnatal supplements because some bottles contain tablets with the wrong identification code.
Tf Supplements is recalling Rhino 7 3000 bottles because they contain undeclared desmethyl carbondenafil and dapoxetine and were marketed without an approved NDA or ANDA.
Tf Supplements is recalling Rhino 7 Platinum 3000 because it contains undeclared desmethyl carbondenafil and dapoxetine and was marketed without an approved NDA or ANDA.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Sufentanil Cit 1000 mcg/ml/Baclofen 300 mcg/ml syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling two syringes of Hydromorphone HCL 1 mg/ml because the agency could not ensure the product was sterile.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Baclofen syringes due to a lack of assurance of sterility. The affected products were distributed nationwide.
Hartley Medical Center Pharmacy is recalling Baclofen 5000 mcg/ml syringes because the agency could not ensure the product was sterile.
Hartley Medical Center Pharmacy is recalling specific hydromorphone, baclofen, and bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate 10 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Hartley Medical Center Pharmacy is recalling two syringes of Morphine Sulfate 0.6 mg/ml due to a lack of assurance of sterility.