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
Toyota is recalling specific 2018-2019 Avalon, Sequoia, Tundra, and Avalon Hybrid vehicles because the air bag software may prevent deployment in a crash.
Suzuki is recalling 2017-2018 DL650, GSX-R1000, and GSX-S750 motorcycles because a twisted fuel pump O-ring may cause a fuel leak, increasing fire risk.
Toyota is recalling 2010-2014 Prius and 2012-2014 Prius V vehicles because excessive voltage may cause the hybrid system to shut down, increasing crash risk.
Johnston County Hams is recalling approximately 89,096 pounds of ready-to-eat ham products due to possible Listeria monocytogenes contamination. The recall affects products distributed in five states.
Zakah Life LLC is recalling Super Green Maeng Da Premium Kratom supplements because FDA samples tested positive for Salmonella.
Hetero Labs Limited is recalling 98,016 bottles of Montelukast Sodium 10 mg tablets because one lot may contain Losartan Potassium 50 mg tablets.
Gravel Ridge Farms is recalling approximately 55,000 dozen shelled eggs due to Salmonella contamination. The products were distributed in Alabama, Georgia, and Tennessee.
Zakah Life LLC is recalling specific batches of Powerful Red Vein Bali Premium Kratom supplements because FDA testing found potential Salmonella contamination.
Bausch & Lomb is recalling Stellaris Elite 23 GA Vit Cutters because the back cap may separate from the body of the device.
Boston Scientific is recalling ESSENTIO pacemakers and CRT-P systems due to an elevated potential for early replacement caused by hydrogen-induced accelerated battery depletion.
Zakah Life LLC is recalling Top Shelf White Maeng Da Premium Kratom supplements because the ingredient lacks safety assurance and red/green strains are potentially contaminated with Salmonella.
Confidence Inc. is recalling For-Men-10 dietary supplements because they contain undeclared ingredients, including HPMC and artificial colors.
Swanson Health Products is recalling Himalayan Crystal Salt because it may contain metal wire pieces. The product was distributed nationwide and in Canada and Switzerland.
Motor Coach Industries is recalling 2018-2019 MCI J4500 motorcoaches with 60-passenger seating due to insufficient emergency egress windows, which may delay passenger exit during an emergency.
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.
Boston Scientific is recalling specific ACCOLADE pacemakers and CRT-P systems due to an elevated potential for early replacement caused by hydrogen-induced accelerated battery depletion.
Boston Scientific is recalling PROPONENT pacemakers because hydrogen exposure may cause the battery to deplete faster than expected, requiring early replacement.
Biomet UK Ltd. is recalling specific HipLOC hip fracture fixation system plates due to an undersized bore that prevents the lag screw from fitting.
Agfa N.V. is recalling 108 DX-D 600 X-ray systems because support cables may break, posing a risk of the equipment falling.
Bausch & Lomb is recalling Stellaris Elite 20 GA Vit Cutters because the back cap may separate from the body of the device.
GE Medical Systems is recalling 516 Discovery MR750w MRI systems because a small area on the bore surface can become warm enough to cause a serious burn if a patient touches it without proper padding.
Winnebago is recalling 2017-2019 Minnie Drop trailers because a missing clamp may allow the propane line to contact the refrigerator burner, posing a fire risk.
Chrysler is recalling 2018-2019 Jeep Wranglers because improperly welded front track bar brackets may separate, reducing steering capability and increasing crash risk.
BMW is recalling 2019 X6 and X6 M vehicles because improperly hardened rear suspension bolts may break, increasing crash risk.
KZRV is recalling 2017-2019 Sonic 190VRB travel trailers because the liquid propane manifold may be located close to the axle tube, posing a fire risk.