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
Shanghai United Imaging Healthcare is recalling three uMI Panorama GS PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans.
Philips North America is recalling 131 MR 5300 systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction.
Alere San Diego, Inc. is recalling multiple hCG pregnancy test models because they may detect low hCG levels, resulting in false positive results.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Philips is recalling SmartPath MRI software because it exports incorrect diffusion tensor imaging data, preventing correct processing by third-party tractography software.
Philips is recalling 340 Ingenia MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate third-party processing.
Shanghai United Imaging Healthcare is recalling three uMI Panvivo PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans.
ASP Global, LLC. 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 Ingenia 1.5T MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate processing by third-party software.
ASP Global, LLC. is recalling 36 units of Expressaire Disposable BB 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 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, 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, LLC. is recalling 400 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Olympus is recalling 543 DisplayPort cables used with the OLYSENSE Hub System because they may cause video dropouts or blackouts during high-power operation.
ASP Global, LLC. 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, LLC. 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, 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.
Percussionaire Corporation is recalling IPV-2C and Phasitron 5 devices to update labeling warnings regarding the use of these devices with volatile anesthetic delivery systems.
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, 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.
FDA is recalling 34 United Imaging uMI 550 PET/CT systems due to a software issue that can hide patient images, potentially requiring rescans.
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 91 Evolution MRI systems because Enhanced MR DICOM exports contain incorrect diffusion directions, preventing correct tractography reconstruction.
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.