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 91 vials of compounded methylprednisolone after seven reports of skin abscesses.
Main Street Family Pharmacy is recalling 10 units of Lipotropic 1.5ml PFS due to adverse reactions reported for a related compounded product.
Main Street Family Pharmacy is recalling Lidocaine 4%/Phenylephrine 1% 5 due to adverse reaction reports linked to a related compounded product.
Main Street Compounding Pharmacy is recalling Taper Pack B after receiving seven reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy is recalling Lipotropic 50ml vials due to seven reports of skin abscesses linked to a related compounded product.
Main Street Compounding Pharmacy is recalling Betamethasone 10mg 10ml vials after seven reports of skin abscesses potentially linked to the product.
Main Street Compounding Pharmacy is recalling Testosterone Cypionate vials due to adverse reactions reported with a different compounded product.
Main Street Family Pharmacy is recalling compounded preservative-free methylprednisolone vials due to reports of skin abscesses.
Main Street Compounding Pharmacy is recalling 66 units of Triamcinolone Acetonide 40mg/ml after receiving reports of skin abscesses.
Main Street Family Pharmacy is recalling compounded preservative-free methylprednisolone vials due to reports of skin abscesses.
Hospira is recalling 29,700 vials of Morphine Sulfate Injection because a confirmed report indicated vial neck breakage caused leakage, compromising sterility.
Main Street Compounding Pharmacy is recalling Lipotropic 10ml with B-12 and L-Carnitine due to reports of skin abscesses linked to a related compounded product.
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.
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.