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
Main Street Family Pharmacy is recalling 313 units of Medroxyprogesterone 150mg vials after receiving seven reports of skin abscesses.
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, LLC is recalling MALE HCG Pk after receiving seven reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy is recalling HCG 220 iu prefilled syringes due to reports of adverse reactions involving skin abscesses.
Main Street Family Pharmacy is recalling compounded methylprednisolone vials after seven reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy is recalling 43 units of HCG Nasal Spray due to adverse reaction reports.
Main Street Family Pharmacy is recalling Estradiol Pellets 25mg after receiving reports of skin abscesses linked to a different compounded product.
Main Street Family Pharmacy is recalling compounded preservative-free methylprednisolone vials due to seven reports of skin abscesses.
Main Street Family Pharmacy is recalling Lipo Blast compounded injections due to reports of skin abscesses.
Main Street Family Pharmacy is recalling Sodium Tetradecyl Sulfate 2.0% 30ml vials due to reports of skin abscesses linked to a related compounded product.
Main Street Compounding Pharmacy is recalling Glycolic 70% gel after receiving reports of skin abscesses linked to a different compounded product.
Main Street Family Pharmacy is recalling 15 units of Adenosine Monophosphate due to adverse reaction reports involving a different compounded product.
Main Street Family Pharmacy is recalling 116 units of B-12 prefilled syringes following reports of skin abscesses linked to a related compounded product.
Main Street Family Pharmacy is recalling 8 units of Lipotropic 30ml vials after receiving seven reports of skin abscesses potentially linked to the product.
Main Street Compounding Pharmacy is recalling preservative-free methylprednisolone vials after seven reports of skin abscesses.
Main Street Family Pharmacy is recalling 107 units of Testosterone Pellets 25mg due to adverse reaction reports.
Main Street Family Pharmacy is recalling HCG 3000IU vials after receiving reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy, LLC is recalling 370 units of Mitomycin 40mg after receiving seven 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 Family Pharmacy is recalling 48 units of Triamcinolone Diacetate 40mg 5ml after receiving reports of skin abscesses.
Main Street Family Pharmacy is recalling 5 units of Calcium Gluconate 2.5% Gel due to adverse reactions reported for a different compounded product.
Main Street Family Pharmacy is recalling compounded preservative-free methylprednisolone vials due to reports of skin abscesses.
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.
Hospira Inc. is recalling 681,400 vials of Ondansetron Injection because glass spicules were found during a site inspection.