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
Daimler Trucks North America is recalling 2017-2018 Thomas Built Buses Saf-T-Liner HDX transit buses because a loose steering pinch bolt may cause loss of vehicle control.
Ford is recalling 2016-2017 Edge, MKX, and Continental vehicles because the driver's air bag may not fully inflate or detach during a crash.
Halcore Group is recalling 2017 Horton ambulances because overtightened rear brake bolts may cause loss of braking power, increasing crash risk.
Halcore Group is recalling 2017 AEV Traumahawk ambulances because overtightened rear brake bolts may cause loss of braking power, increasing crash risk.
Daimler Trucks North America is recalling 2017-2018 Thomas Built Buses Saf-T-Liner HDX school buses because a loose steering bolt may cause loss of vehicle control.
Forest River is recalling 2017 Sandstorm and Stealth recreational vehicles because the liquid propane line may be damaged by the axle, creating a fire or explosion hazard.
Forest River is recalling 2017 Wildwood and Salem recreational trailers because an improperly installed refrigerator vent allows propane gas to enter the vehicle, increasing the risk of fire or explosion.
Little Tikes is recalling about 540,000 2-in-1 Snug 'n Secure Pink toddler swings because the plastic seat can crack or break, posing a fall hazard.
Carrier is expanding a recall for about 94,000 packaged terminal air conditioners and heat pumps because the power cord plug can overheat, posing a fire hazard.
Giant Eagle is recalling Apple Pistachio Salad due to potential Listeria monocytogenes contamination. Consumers in Ohio and Pennsylvania should not eat the product.
MS Bionic is recalling MegaJex Herbal Supplement because it contains sildenafil and tadalafil, active ingredients in approved erectile dysfunction drugs, without FDA approval.
Ready Pac Foods is recalling approximately 59,225 pounds of Puro Picante Blazin Hot chicken salad due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Giant Eagle is recalling Apple Pistachio Salad with Chicken due to potential Listeria monocytogenes contamination. The product was sold in Ohio and Pennsylvania.
Whole Foods Market is recalling specific Key Lime Tarts because they contain almond flour, a tree nut, which is not listed on the store scale label.
GE Healthcare is recalling 60 Discovery MR450 MRI scanners because a component failure can cause the patient bore to heat up, potentially leading to serious burns.
Whole Foods Market is recalling Tart Peanut Butter Chocolate because almond flour is missing from the scale label, posing a risk to consumers with nut allergies.
Whole Foods Market is recalling tart crusts because almond flour is missing from the scale label, posing a risk to people with nut allergies.
Integra LifeSciences Corp. is recalling 944 units of the Cadence Total Ankle System because posterior tibial fractures have been reported.
Whole Foods Market is recalling Tart French Apple Small tarts because almond flour is not listed on the scale label, posing a risk to people with nut allergies.
Physio-Control is recalling 338 LIFEPAK 15 defibrillators because an internal relay may fail, preventing the device from delivering defibrillation energy.
Siemens is recalling 194 PRIMUS radiation therapy systems due to incorrect collimator position displays and improper weld seams at the overhead suspension.
Whole Foods Market is recalling specific tart products because almond flour is not listed on the scale label, posing a risk to consumers with nut allergies.
Whole Foods Market is recalling Tart Lemon Small products because almond flour is not listed on the scale label, posing a risk to consumers with nut allergies.
Mako Surgical Corporation is recalling 595 Stryker Restoris RIO Reamer Handles because they may fail to engage mating components during surgery.
Jersey Shore Supplements, LLC is recalling SLIMFIT X capsules because they contain undeclared sibutramine and desmethylsibutramine and were marketed without an approved NDA/ANDA.