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
Ford is recalling 2018 Expedition, F-150, and Lincoln Navigator vehicles because a fuel pump weld can fracture, causing a leak that increases fire risk.
Lamborghini is recalling 2012-2018 Aventador vehicles because the engine may stall unexpectedly, increasing crash risk. Dealers will install updated software.
Ford is recalling 2017-2018 Edge and 2017 Lincoln MKZ vehicles because inadequate welding on the torque converter may cause the vehicle to lose the ability to move, increasing crash risk.
Ford is recalling 2018 F-650 and F-750 trucks because brake hose fittings may lack anti-corrosion plating, risking fluid leaks and reduced braking.
BMW is recalling specific 2000-2006 models because the passenger air bag inflator may rupture during deployment, potentially sending metal fragments into the cabin.
Venda Ravioli, Inc. is recalling approximately 672 pounds of frozen meat ravioli products produced without the benefit of federal inspection. The products were distributed to retail locations in Massachusetts and Rhode Island.
Forest River is recalling 2019 Salem and Wildwood recreational trailers because an axle equalizer defect could cause axle failure and increase crash risk.
Thor Motor Coach is recalling 691 specific 2019 motorhome models because rear axle U-bolts may be insufficiently tightened, posing a risk of axle separation and loss of control.
Keystone is recalling 2018-2019 Cougar recreational trailers because the wooden assembly of the outdoor propane grill may lack sufficient clearance, increasing fire risk.
Spartan is recalling 2016-2019 K2 and K3 motorhome chassis because the tag axle tire may be damaged by the DEF fill bracket, increasing crash risk.
Supermercado Selectos is recalling raw, frozen fish, beef, pork, and poultry products produced without federal inspection. No illnesses have been reported.
Ferrari is recalling 2012 California, 458, and FF models because the passenger air bag inflator may explode in a crash, potentially causing serious injury or death.
Caudill Sprouting LLC is recalling alfalfa seeds linked to a multistate outbreak of Salmonella Montevideo and Salmonella Cubana infections.
Shoreside Enterprises Inc. is recalling Poseidon Xtreme PLATINUM 4500 because FDA analysis found undeclared sildenafil and tadalafil, making it an unapproved drug.
The FDA is recalling 7K capsules distributed by SX Power Co. because they contain undeclared sildenafil and tadalafil, making them unapproved drugs with unestablished safety and efficacy.
Maquet Datascope is recalling CARDIOSAVE Hybrid Intra-Aortic Balloon Pumps because fluid ingress can damage electronic circuit boards, preventing therapy initiation or continuation.
Northwood is recalling 2019 Nash 24M and 29S travel trailers because tires may rub against shocks, causing damage and increasing crash risk.
Ziyad Brothers Importing is voluntarily recalling Ziyad Brand Tahini in various glass jar sizes due to potential Salmonella contamination.
WRP Asia Pacific Sdn Bhd is recalling 201,000 pairs of AmerisourceBergen sterile surgical gloves because some left-handed gloves contain powder, which is banned in the U.S.
Torax Medical is recalling LINX Reflux Management System implant clasps because a manufacturing defect may allow a bead to separate from the wire link, potentially rendering the device open or discontinuous.
Volkswagen is recalling 2018 Atlas and Tiguan vehicles because the passenger frontal air bag may tear or fail to unfold properly in a crash, increasing injury risk.
Philips is recalling five HeartStart MRx monitor/defibrillators because a faulty circuit board may prevent charging, potentially delaying life-saving therapy.
Ethicon Endo-Surgery Inc is recalling HARMONIC ACE Shears because an internal component may cause continuous or inadvertent activation of the device.
Torax Medical is recalling LINX Reflux Management System implant clasps because a manufacturing defect may allow a bead to separate from the wire link, potentially rendering the device open or discontinuous.
Gyrus Acmi is recalling 6,447 reusable active cords for electrosurgical generators due to a potential risk of sparking and causing a fire.