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
Philips is recalling Ingenia 3.0T MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Philips is recalling 107 MR 7700 MRI systems because diffusion tensor imaging (DTI) exports contain incorrect data, preventing accurate tractography reconstruction.
ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Micro Therapeutics is recalling two units of the Pipeline Flex Embolization Device with Shield Technology because the packaging label incorrectly listed the diameter as 3.00 mm when the actual unit was 2.50 mm.
Apotex Corp. is recalling Paroxetine Hydrochloride Extended-Release Tablets, 37.5mg, because they failed dissolution specifications.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling 80 MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is 5 years.
ASP Global, LLC. is recalling 180 units of MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Philips is recalling 30 MR 7700 software upgrades because they export incorrect diffusion tensor imaging data, preventing accurate nerve fiber mapping.
HeartSine Technologies is recalling 31,834 public access defibrillators distributed without the required Maintenance Supplement, which describes an extra check every 3 months.
Karl Storz Endoscopy is recalling six HOPKINS Telescope eyepieces because of incorrect inside packaging labels. The units were distributed in Arizona, California, and Missouri.
Ford is recalling certain 2025-2026 F-Series trucks because the speedometer and tachometer may display inaccurate readings, increasing crash risk.
Great Dane is recalling 2027 Champion dry van trailers because an incorrect coupler plate may prevent proper coupling, increasing crash risk.
Chrysler is recalling 2026 Ram 2500 trucks because steering column modules may cause a loss of electronic stability control, increasing crash risk.
Ford is recalling 2025-2027 F-150 vehicles because front seats may be improperly secured, increasing injury risk in a crash. Dealers will inspect and repair the seats free of charge.
E-One is recalling specific Typhoon N, Cyclone N, and Cyclone II fire trucks because a loose power supply may cause wiring to overheat, increasing fire risk.
KME is recalling 2024 CV515 SFA 4x4 and Severe Service emergency vehicles because a node may become unresponsive, causing loss of exterior lighting and pump-mode functionality.
Ford is recalling 2015 Transit Connect vehicles because the rearview camera may display a distorted or blank image, increasing crash risk.
Spartan Fire is recalling one 2024 Metrostar emergency vehicle because a node may become unresponsive, causing loss of exterior lighting or pump-mode functionality.
USDA FSIS issued a public health alert for canned chicken sausages illegally imported from Jamaica. Consumers in five states should discard the products.
Kalmar is recalling 2014-2026 Ottawa T2 terminal tractors because damaged circuit board insulation may cause a short circuit and fire. Owners should park vehicles outside until repaired.