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
Health Innovations Pharmacy is recalling DNCB 0.3% Ointment due to lack of assurance of sterility and stability data. The recall covers all lots distributed in North Carolina.
Blue Bird is recalling 2009-2016 All American non-school buses due to a defect that may allow engine oil to contact hot surfaces, increasing fire risk.
Tiffin is recalling specific 2015 Allegro and Phaeton motorhomes because moisture may cause slide-out sections to extend while driving, increasing crash risk.
Blue Bird is recalling 840 school buses due to a defect that may allow engine oil to contact hot surfaces, increasing fire risk.
NABI is recalling 2007-2015 LFW, BRT, and 2007-2013 CLFW transit buses because a vent tube may detach, allowing engine oil to contact hot surfaces and cause a fire.
Takata is recalling specific frontal driver air bag inflator modules that may rupture during deployment, potentially causing serious injury or death.
Takata is recalling specific frontal passenger air bag inflators for certain Honda and Mazda vehicles due to a risk of rupture during deployment.
Takata is recalling PSPI-L passenger air bag inflators in specific Honda, Toyota, Pontiac, and Subaru models. The inflators may rupture in a crash, sending metal fragments into the vehicle.
Autocar is recalling 2011-2016 Xpeditor vehicles because the parking brake may engage unexpectedly at any speed, increasing crash risk.
Chrysler is recalling 2014-2015 RAM 4500 and 5500 trucks because their tires are rated for a lower speed than the vehicle's maximum capability, posing a crash risk.
ZYK Enterprises is recalling 2,522 pounds of boneless veal trim and whole muscle cuts due to possible E. coli O157:H7 contamination. The products were distributed to wholesale establishments in California, Massachusetts, and Washington.
Takata is recalling specific passenger frontal air bag inflators for 2001-2008 vehicles due to a risk of rupture during deployment.
Daimler Buses North America is recalling 2007-2012 Orion VII natural gas buses because engine oil may contact hot surfaces, increasing fire risk.
Nissan is recalling specific 2001-2006 models because the passenger air bag inflator may rupture during deployment, potentially sending metal fragments into the vehicle.
Industrial Axle Company is recalling specific ALKO AXIS trailer axles because wheel mounting studs may fail, potentially causing wheel separation and increasing crash risk.
Physician Preferred Medical, LLC is recalling Epel 18 mg Estradiol Pellets because the specific lot failed sterility testing. The product was distributed in Arizona and Kansas.
La Terra Fina is recalling specific lots of Chunky Spinach Artichoke & Parmesan Dip because the chopped spinach ingredient tested positive for Listeria monocytogenes.
Detox Transforms is recalling EDGE Amplified Weight Release capsules because the product contains undeclared phenolphthalein and fluoxetine, making it an unapproved drug.
Ultra ZX Labs is recalling Ultra ZX dietary supplements because FDA testing found undeclared sibutramine and phenolphthalein. The product was marketed without an approved NDA or ANDA.
The FDA is recalling iNSANE Bee Pollen capsules because they contain undeclared phenolphthalein and fluoxetine, making them unapproved drugs.
REFA Enterprises is recalling Forever Beautiful Bee Pollen capsules because FDA analysis found the product contains sibutramine and phenolphthalein.
REFA Enterprises is recalling Forever Beautiful INFINITY capsules because FDA analysis found the product contains sibutramine and phenolphthalein without an approved NDA/ANDA.
Anabolic Science Labs LLC is recalling Estrastain Pro-Anabolic Mass and Hardening Complex capsules because they contain unapproved synthetic hormone ingredients.
La Terra Fina is recalling Organic Thick & Creamy Spinach Dip and Spread because the chopped spinach ingredient tested positive for Listeria monocytogenes.
Anabolic Science Labs is recalling SWOLL-250 Super Mass Builder Quad Stack capsules because they contain unapproved synthetic hormone ingredients.