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
Lucid is recalling 2022-2023 Air vehicles where the rearview camera may fail to display in reverse, violating safety standards. A free over-the-air software update will fix the issue.
Software versions 2.0.64 and older in 2022–2023 Lucid Air vehicles may not respond properly to inverter failures, causing sudden loss of drive power without warning. This increases the risk of crashes.
GAF Energy is recalling about 2,100 Timberline Solar Energy Shingles (TLS-1) due to electrical component malfunction that poses a fire hazard. One fire and five thermal incidents resulting in property damage have been reported, with no injuries.
Hyundai is recalling 2023-2024 Palisade and Tucson vehicles, plus 2023 Sonata, Elantra, and Kona models for defective oil pump controllers that may overheat and increase fire risk. Owners should park outside until repairs are complete.
Airstream is recalling certain 2023-2024 travel trailers because the SmartPlug 30-amp inlet D-rings may crack when over-tightened, risking electrical arcing and fire.
Jaguar is recalling 2021-2022 I-Pace vehicles due to a faulty high voltage coolant heater that fails to defrost the windshield. This can reduce driver visibility and increase crash risk.
The 2022-2023 Lucid Air may have loose windshield wiper arm nuts, causing the wipers to fail and reducing visibility. No injuries have been reported.
Certain 2024 Porsche Cayenne models may fail to illuminate rear hazard warning and parking lights when activated shortly after engine shutdown. This defect reduces vehicle visibility and increases crash risk.
Honda CR-V vehicles from 2017, 2020, and 2022 are being recalled for an incorrect driver's door label with wrong tire size and weight ratings. Incorrect tire information may cause premature wear or tire blowout, increasing crash risk.
SunOpta Grains and Foods Inc. is recalling frozen cherries sold under Great Value, Good & Gather, and Best Choice brands nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.
Olympus is recalling 17,609 bronchovideoscope units nationwide due to complaints of endobronchial combustion during therapeutic laser procedures, which poses a fire and burn risk to patients.
365 Whole Foods Market Organic Tropical Fruit Medley is recalled nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume this product.
Olympus bronchoscopes (Models BF-PE2 and BF-TE2) are recalled due to reports of combustion inside the airway during laser-assisted medical procedures. This is an FDA Class I recall.
Abiomed is recalling Impella CP with SmartAssist blood pumps due to risk of motor housing interaction with transcatheter aortic valve replacement devices, which can damage the pump's impeller blades and reduce blood flow.
Olympus is recalling EVIS EXERA III Bronchovideoscopes nationwide due to complaints of endobronchial combustion during therapeutic laser procedures. This FDA Class I recall affects approximately 9,684 units.
Rose Street Bread Lab is recalling 27 loaves of Rose Street Patisserie Multi Grain Bread due to undeclared sesame. Consumers with sesame allergies risk serious allergic reactions.
Whole Foods Market is recalling 365 brand organic blackberries due to potential Listeria monocytogenes contamination. The frozen fruit was distributed nationwide.
SunOpta Grains and Foods Inc. is recalling 365 Whole Foods Market Organic Whole Strawberries due to potential Listeria monocytogenes contamination. The frozen strawberries were distributed nationwide.
SunOpta Grains and Foods Inc. is recalling 365 Whole Foods Market Organic Sliced Strawberries & Bananas due to potential Listeria monocytogenes contamination. The frozen fruit products were distributed nationwide.
Datascope has recalled Cardiosave Hybrid IABP models due to tantalum capacitor failures that may cause unexpected device shutdown, interrupting life-critical cardiac therapy.
Townsend Farms Inc is recalling Private Selection frozen tropical mango chunks due to potential Listeria monocytogenes contamination. The product was distributed across 16 U.S. states.
Target's Good & Gather frozen blueberries are being recalled nationwide due to potential Listeria monocytogenes contamination affecting approximately 3,894 cases.
Olympus is recalling 9 bronchoscopes (Models BF-P150 and BF-1T150) due to complaints of endobronchial combustion during therapeutic laser procedures. The defect could cause fire and serious burn injuries.
Abiomed recalls Impella LD blood pumps due to potential interaction with aortic valve replacement devices that can damage the pump impeller and cause blood clots. Patients with these devices should contact their healthcare provider.
Walmart's Great Value Mixed Fruit is recalled for potential Listeria monocytogenes contamination. The FDA issued a Class I recall affecting approximately 70,360 cases distributed nationwide.