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 deaths or serious injuries are reported, 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
Cardinal Health is recalling 375 OptiChamber Diamond Spacer devices due to temperature exposure during shipping that may cause inaccurate medication delivery results. Affected devices were distributed to Florida, Georgia, and South Carolina.
Exact Medical Manufacturing is recalling 33,250 ultrasonic transducer probe covers lacking required FDA 510(k) clearance for use in natural or surgical body openings, distributed to Florida, Montana, New York, Ohio, Georgia, and Puerto Rico.
VanLeigh is recalling 2021-2022 Beacon recreational vehicles because a rear ladder can interfere with the rear egress window, preventing it from fully opening in emergencies.
Porsche is recalling certain 2020-2021 Taycan models due to a software monitoring fault that can incorrectly shut down the powertrain, causing loss of motive power and increasing crash risk.
Daimler Trucks North America is recalling certain Freightliner and Western Star trucks because the battery cable terminal may break, causing engine stall and crash risk. Dealers will repair or replace the cables at no cost.
Winnebago is recalling certain 2021-2022 Solis, Travato, and Ekko models equipped with GE-ES Double Flipseats because seat belt retractors may lock when the vehicle is on a slight incline, creating risk that passengers may feel trapped.
Mercedes-Benz is recalling certain 2021-2022 vehicles because rear seat belt automatic locking retractors may deactivate early, preventing child restraint systems from securing properly. An unsecured child restraint increases the risk of injury during a crash.
Roadtrek is recalling certain 2020-2021 Zion, Zion SRT, Play, and Slumber vehicles equipped with a faulty gas detector missing a carbon monoxide alarm. Undetected carbon monoxide can cause serious injury or death.
Certain 2021 Nissan Rogue vehicles have improperly welded upper tether attachment points in the rear seat. This defect prevents child safety seats from being properly anchored, increasing injury risk during crashes.
Plant Guru is recalling about 25,600 units of wintergreen, birch, and essential oil blend products because the packaging is not child-resistant despite containing methyl salicylate, which poses a poisoning risk if swallowed by young children.
Gramr is recalling about 92,135 Brushed Gold Tea Kettles because they can expel hot water and excessive steam during use, posing a burn hazard. The company has received 122 reports of the kettles expelling hot water or steam, including 18 reports of minor burn injuries.
General Motors is recalling certain 2021 Buick Enclave and Chevrolet Traverse vehicles due to potentially incorrect air bag calibration software that may affect frontal air bag deployment.
La Paloma is recalling about 70 girls' nightgowns sold online from November through December 2020 because they fail to meet federal flammability standards for children's sleepwear, posing a burn hazard. No injuries have been reported.
HMO Beverage Corp. dba Organic Gemini LLC is recalling Organic Gemini TigerNut Flour (27.5 lb bags) because the product may be contaminated with Salmonella. Consumers should not consume the affected product.
Natural Foods Inc is recalling BulkFoods.com brand dehydrated chopped celery in 1lb and 5lb bags due to potential Salmonella contamination. The affected product was distributed to multiple states.
Olde Thompson and Sun Harvest are recalling 1.5oz. jars of organic ground coriander due to potential Salmonella contamination. Affected lots are 23631 and 23632 with best-before dates of 05/2023.
Imperia Elita Vitaccino Coffee sachets are being recalled because they were marketed without FDA approval and contain pharmaceutical ingredients Sibutramine and Fluoxetine. All lots distributed nationwide are affected.
Medtronic Vascular recalled 54,997 angiographic guidewire components that were shipped directly to customers without the required downstream processing and sterilization. The components should have been sent to a third-party processor first.
Medtronic has recalled 16 tubing packs from its CB10R79R6 Custom Perfusion System due to insufficient or incomplete welds in specific lots. The defect may compromise device integrity during use.
Tiger Nuts is recalling Tiger Nuts Flour 2.2 lb boxes due to potential Salmonella contamination. The affected product was distributed in Oregon, Missouri, Kansas, and nationwide through e-commerce.
Medtronic is recalling specific lots of CB4W67R20 Custom Perfusion System tubing packs due to incomplete welds that could affect system performance. The recall affects 61 packs distributed across nine states.
Ossur Americas is recalling the MIAMI J SELECT COLLAR cervical spine device due to deforming racks that may reduce immobilization. About 10,469 units were distributed nationwide.
Medtronic Perfusion System tubing packs are recalled due to manufacturing defects involving insufficient or incomplete welds in the CB10W63R1 lot. Affected devices may malfunction during use.
Savor Brands LLC. is recalling Brown Rice Quinoa Farro (24 lb cases) because the product fails to declare wheat, a major food allergen, on the label. Approximately 4,597 cases were distributed to restaurants via a distributor in Illinois.
The Better-Bladder ECMO device used in cardiopulmonary bypass circuits may collapse during use, increasing venous line resistance and reducing blood flow. The recall affects 147 units distributed nationwide.