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
Main Street Family Pharmacy is recalling compounded preservative-free methylprednisolone 80mg/ml 10 ml vials due to reports of skin abscesses.
Main Street Family Pharmacy is recalling 9 units of Betamethasone 6.5mg 10ml vials after seven reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy is recalling 313 units of Medroxyprogesterone 150mg vials after receiving seven reports of skin abscesses.
Main Street Family Pharmacy, LLC is recalling HCG and methylprednisolone products due to reports of skin abscesses.
Main Street Family Pharmacy is recalling Estradiol Pellets 31mg after receiving reports of skin abscesses linked to a different compounded product.
W.S. Badger Company is recalling specific lots of Badger Kids Sunscreen Lotion due to microbial contamination. The product was distributed in the US, Canada, and several other countries.
W.S. Badger Company Inc. is recalling specific lots of Badger Baby and Kids Sunscreen Lotion due to microbial contamination.
Jack Rabbit, Inc. is recalling its J.R. Jack Rabbit All Natural Herbal Supplement because FDA testing found undeclared sildenafil and tadalafil.
Actavis Elizabeth LLC is recalling 756 bottles of Alprazolam 2 mg tablets because some tablets weighed less than the required specification.
Apotex Inc. is recalling 4,844 bottles of Acyclovir 800 mg tablets (Lot KF2199) because some tablets may contain embedded pieces of nitrile rubber glove.
Cetylite Industries is recalling Cetacaine Topical Anesthetic Liquid because the tetracaine ingredient is below specification limits at the 21-month stability test point.
Novartis Consumer Health is recalling 11.8 million loratadine 10 mg antihistamine blister packs sold nationwide under seven different store brands because the tablets are chipped or broken.
Fresenius Kabi USA, LLC is recalling 71,129 vials of Paclitaxel Injection because the package insert is missing text in the Clinical Studies and Specific Adverse Events sections.
Valeant Pharmaceuticals is recalling 45,000 tubes of Acanya gel physician samples because they were assigned an incorrect expiration date.
Teva Pharmaceuticals is recalling 6,803 cartons of Copaxone pre-filled syringes because a foreign particle was found in one unit.
Greenstone LLC is recalling 4,848 bottles of Spironolactone 50 mg tablets because the manufacturing site change resulted in an unapproved dissolution profile.
Affirm XL is recalling its nutritional supplement because FDA analysis found it contains sulfoaildenafil, an unapproved analogue of sildenafil.
Hospira Inc. is recalling 251,400 vials of Metoclopramide Injection because glass spicules were found during a site inspection.
Hospira Inc. is recalling 681,400 vials of Ondansetron Injection because glass spicules were found during a site inspection.
Boehringer Ingelheim is recalling 10,267 bottles of Oxcarbazepine Oral Suspension because the product failed to meet resuspendability requirements.
L. Perrigo is recalling 108,828 bottles of infants' acetaminophen because some cartons may contain dosing syringes without dose markings.
Kremers Urban Pharmaceuticals is recalling 3,867 bottles of Omeprazole 20 mg capsules because some may not meet acid resistance specifications.
Pfizer is recalling Aldactone (spironolactone) 100 mg tablets because the manufacturing site change resulted in an unapproved dissolution profile.
L. Perrigo Co. is recalling 143,892 bottles of infants' acetaminophen suspension because some may be packaged with dosing syringes lacking dose markings.
Greenstone LLC is recalling 2,796 bottles of Spironolactone 25 mg tablets because they were manufactured at an unapproved site, altering the dissolution profile.