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
Max-Trac is recalling specific Avon Viper Stryke tires because a tread bulge or separation could cause loss of vehicle control and increase crash risk.
Kia is recalling 2014-2016 Soul and Soul EV vehicles because a pinion plug defect may allow the pinion gear to separate, potentially causing loss of steering and increasing crash risk.
Mitsubishi is recalling 2015-2017 Outlander, Outlander Sport, Lancer, and Lancer Evolution vehicles because defective relays may cause engine stalls, reduced power, or overheating.
Hino is recalling 3,224 trucks because worn engine parts may cause failure, increasing crash risk.
BMW is recalling 2006-2010 X3 vehicles because the front passenger seat occupant detection mat may crack, potentially deactivating the air bag in a crash.
Silver Eagle is recalling 2018 Vast-20W converter dolly trailers because brake caliper bolts may not be properly torqued, risking caliper detachment and loss of braking ability.
Dierbergs Markets is recalling Scampi Butter because it contains undeclared fish and crustacean shellfish. Consumers with allergies should not consume the product.
Bravo Produce Inc is recalling Maradol papayas due to Salmonella contamination. The product was distributed in California.
Kelejete LLC is recalling Cranberry Raisin Jete Nutritional Energy Bars because the label failed to declare peanuts and pecans in the 'Contains' statement.
Sunopta Grains and Foods is recalling Organic Great Value Dark Sweet Cherry Products Pitted because testing found Listeria monocytogenes in a finished product sample.
Medtronic Navigation is recalling Spine Referencing Instrumentation sets due to a risk that clamps may break during use, potentially leaving components in the patient's body.
Dierbergs Markets is recalling Cabernet Grille Butter because it contains undeclared wheat and soy allergens.
Wabash is recalling 2012-2013 converter dolly trailers because fasteners may loosen, allowing the counterweight tube to detach while in motion, increasing crash risk.
America New York RI Wang Food Group is recalling approximately 63,823 pounds of pork and beef sausage products due to misbranding and an undeclared milk allergen.
Medtronic Navigation is recalling Spine Referencing Instrumentation, Double Spinous Process Clamp, Tall units due to a risk of component breakage or damage during use.
Simply Fresh Foods is recalling San Francisco Foods Seafood Salad with Greek Yogurt because the ingredient label may fail to declare milk as an allergen.
Medtronic is recalling Spine Referencing Instrumentation clamps due to a risk of breakage that could leave components in the patient's body.
Medtronic is recalling Spine Referencing Instrumentation because the clamps may be damaged if opened beyond limits, potentially leaving components in the patient.
Pfizer is recalling specific lots of Levophed (norepinephrine bitartrate) injection because a damaged sterilizing filter may have compromised sterility.
Kelejete LLC is recalling 136 Chocolate Jete Nutritional Energy Bars because the label failed to declare peanuts and pecans in the 'Contains' statement and omitted sulfites.
Medtronic is recalling Spine Referencing Instrumentation, Double Spinous Process Clamp, Short units because they may break during use, potentially leaving components in the patient's body.
Kelejete LLC is recalling Dark Chocolate Jete Nutritional Energy Bars because the label failed to declare peanuts and pecans in the 'Contains' statement.
Pfizer is recalling 115,370 vials of Hydromorphone Hydrochloride Injection because a damaged sterilizing filter may have compromised sterility assurance during manufacturing.
Genentech is recalling 16,882 units of Activase (alteplase) because the included sterile water vials may have cracked or chipped glass.
Polar Tank is recalling 2018 SRJ7 trailers because brake caliper bolts may not be properly torqued, risking caliper detachment and loss of braking ability.