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
Keystone RV Company is recalling certain 2022 Alpine and Avalanche vehicles due to improperly secured exterior ladders that may detach while in use, creating a risk of injury.
Tenneco Automotive is recalling aftermarket ball joints for 2004-2007 Toyota Sequoia and 2004-2006 Toyota Tundra vehicles due to potential premature failure.
KTM is recalling 2022 Husqvarna FE 350S and FE 501S motorcycles because incorrectly mounted front brake pad retaining clips may cause pads to detach, reducing braking performance.
Ford is recalling certain 2021 diesel trucks due to a void in the secondary fuel filter cap that may leak fuel, posing a fire risk. Dealers will replace the fuel filters free of charge.
Forest River is recalling certain 2022 Cherokee toy haulers because the Tire and Loading Information placard may show incorrect rim specifications, potentially causing improper tire installation and crash risk.
Volta Power Systems is recalling 646 adaptor harnesses because incorrect construction may cause overheating and fire.
Ford is recalling 2014-2015 Fusion, Lincoln MKZ, and 2015 Mustang vehicles because brake pedal bumpers may corrode and separate, potentially causing brake light confusion or rollaway risks.
Seagrave is recalling 2011-2021 Marauder and Capitol firetrucks because a crossmember mounting plate may crack, potentially distracting the driver and increasing crash risk.
Bokhary Foods, Inc. is recalling Godavari brand apricots in 7 oz and 14 oz packages because they contain undeclared sulfites. Consumers allergic or sensitive to sulfites should not consume the product.
Sandridge Food Corporation is recalling Macaroni & Cheese (Macarrones con Queso) distributed to restaurants and a hotel in Texas because the product contains egg but does not declare this allergen on the label.
Flowers Foods is recalling Nature's Own Honey Wheat Bread due to undeclared milk, which poses a risk to consumers with milk allergies. The product was distributed in Arizona, California, Colorado, New Mexico, Nevada, and Wyoming.
Qiagen Sciences is recalling 376 units of its QIAstat-Dx Respiratory SARS-CoV-2 Panel diagnostic kit due to faulty cartridges that can produce false-negative or false-positive test results.
Invacare power wheelchairs with LiNX Gyro firmware 6.1.2 may decelerate more aggressively than programmed, risking user injury due to an incorrect deceleration profile.
EGL Motor is recalling about 2,900 EGL and ACE branded youth ATVs (models MADIX 125 and D110) because they fail federal safety standards, allowing children to exceed safe speeds and creating laceration and crash hazards.
DiaSorin Molecular's Simplexa Direct Amplification Disc Kit is recalled due to risk of leakage when used multiple times, which may cause cross-contamination in laboratory settings if not properly cleaned.
Abbott Molecular is recalling 742 Alinity m Systems worldwide due to a software defect that can set the Amplification Detection clamp CLEAN position too high, potentially affecting instrument operation.
Abbott Molecular is recalling 74 Alinity m Systems due to an issue with the installation of updated camera firmware. Affected devices were distributed in the United States and internationally.
Trader Joe's Soycutash (Item #99319), a frozen mix of sweet corn, shelled edamame, and red bell peppers, is being recalled because it may be contaminated with Listeria monocytogenes. The recall affects products distributed in Arizona, California, Nevada, and Utah.
About 3,500 children's robes made by HulovoX fail federal flammability standards for sleepwear and pose a burn injury risk. The robes were sold online through Amazon.com from January to May 2021 for about $30 each.
Medshape is recalling DYNANAIL MINI surgical nails due to manufacturing defect in lot 04882. Affected endcaps may not seat flush during surgical insertion, potentially affecting implant integrity.
Joy's International Foods is recalling Joy's Gourmet Blast Off! Bloody Mary Mix (24 oz) due to undeclared fish and soy allergens. Consumers with allergies to these ingredients should not consume the product.
Abbott Molecular is recalling 742 Alinity m System units worldwide due to a software issue that prevents Field Service Engineers from properly completing maintenance and diagnostics procedures.
Siemens is recalling Atellica CH 930 clinical chemistry analyzers with software v1.25.1 or lower. Two software defects could cause inaccurate test results: test parameters may revert to defaults, or the analyzer may use expired reagents.
Some Invacare AVIVA FX power wheelchairs with LiNX Gyro firmware 6.1.2 may decelerate more aggressively than programmed, creating injury risk.
Uromedica is recalling nonsterile implantation instrument sheaths (Lot UM00794 and UM00817) because the U-channel sheaths may damage ProACT implant devices during implantation procedures. Affected devices were distributed nationwide.