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
AA USA Trading Inc. is recalling 8-ounce packages of Ginger Slices because they contain undeclared sulfites. The product was distributed in New York and New Jersey.
R Thomas Marketing, LLC is recalling Night Man capsules because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Black Storm capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Bull's Genital capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Volkswagen Group of America is recalling specific Audi A4 and A6 models because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
M.B. Sturgis is recalling specific propane gas regulators where a cracked window may allow gas to leak, increasing fire risk. Dealers will replace the parts free of charge.
The Sausage Maker, Inc. is recalling Smoked Pepperoni seasoning because the Fermento ingredient contains undeclared whey protein and skim milk powder.
The Sausage Maker, Inc. is recalling Goetburg Summer Sausage seasoning due to undeclared whey protein and skim milk powder.
Akorn, Inc. is recalling PerioRx oral rinse because multiple batches failed impurity specifications. The product contains an unknown impurity of chlorhexidine gluconate.
Teva North America is recalling 546 bags of Linezolid Injection due to potential leaking that compromises sterility.
R Thomas Marketing, LLC is recalling Zhen Gong Fu capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
The FDA is recalling Black Ant supplements distributed by R Thomas Marketing, LLC because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Southwire is recalling approximately 1.2 million non-contact voltage detectors because they may provide false readings, posing shock and burn risks.
Mohu is recalling about 1,700 BeBox smart boomboxes because they can overheat, posing burn and fire hazards. One incident of a unit catching fire was reported, with no injuries.
R Thomas Marketing, LLC is recalling Bull capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Traxxas is recalling X-Maxx Monster Trucks and VXL-6 electronic speed controls because a short circuit can cause a fire. The company reported 40 fires and one injury.
American Surgical Company is recalling Delicot X sponges due to packaging defects that compromise sterility. The recall covers 3 boxes distributed worldwide.
Baxter Healthcare is recalling 282,080 bags of 0.9% Sodium Chloride Injection USP due to a lack of assurance of sterility caused by potential container leaks.
Aloha Medicinals is recalling organic dried mushroom powder after a sample tested positive for E. coli following customer reports of stomach issues.
Hospira Inc. is recalling 72,000 units of 8.4% Sodium Bicarbonate Injection because an insect was found in one vial.
KZRV is recalling 2016 MXT travel trailers because the safety chains are rated for less weight than the vehicle's gross weight rating, posing a crash risk if the main connection fails.
The Sausage Maker, Inc. is recalling specific seasoning products because they contain undeclared whey protein and skim milk powder.
Kia is recalling 2006-2012 Sedona minivans in specific states because front lower control arms may break due to salt water corrosion, increasing crash risk.
The Sausage Maker, Inc. is recalling Summer Sausage seasoning due to undeclared whey protein and skim milk powder.
R Thomas Marketing, LLC is recalling African Superman supplements because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).