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 37 MR 7700 MRI systems due to a software issue that can terminate examinations during image reconstruction.
Philips is recalling 210 Achieva 3.0T MRI scanners because a software issue can terminate examinations if system memory is exceeded during image reconstruction.
Baxter Healthcare is recalling 169 PRO+ MRS Mattresses because UDI label errors may lead to incorrect product identification or use with incompatible bed frames.
Philips is recalling 82 Intera 1.5T MRI systems worldwide because a software issue can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Olympus is recalling 305 units of EZDilate Endoscopic Balloon Dilators because the inflation chart label may incorrectly indicate balloon diameters of 18, 19, or 20 mm.
Philips is recalling 2,038 Ingenia 1.5T MRI systems worldwide due to a software issue that can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Baxter Healthcare is recalling 824 PRO+ 36-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label. The discrepancies may lead to incorrect product identification or use with incompatible bed frames.
AVID Medical is recalling 192 Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.
Kwok Shing, Inc. is recalling 70 boxes of American Ginseng due to potential pesticide contamination. The product was distributed in California.
Philips is recalling SmartPath MRI software due to a defect that can terminate examinations during image reconstruction if system memory is exceeded.
Philips is recalling 15 Achieva XR MRI systems because a software issue can terminate examinations if scan parameters exceed system memory.
Philips is recalling 596 Ingenia Elition MRI systems due to a software issue that can terminate examinations during image reconstruction if system memory is exceeded.
WWF Operating Company is recalling So Delicious Dairy Free Salted Caramel Cluster Cashewmilk because it may contain small stones and other hard objects.
AVID Medical is recalling Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.
Ventec Life Systems is recalling 21 HomeFill Oxygen System cylinders because they lack required medical gas labeling.
Macleods Pharmaceuticals is recalling Olanzapine 5 mg tablets because organic and unspecified impurities exceeded specifications.
Chrysler is recalling MOPAR body and jumper wiring harnesses because water intrusion can disable electric power steering assist, increasing crash risk.
Rivian is recalling 2027 R2 vehicles because a high voltage battery fastener may be improperly tightened, which can cause a loss of drive power and increase crash risk.
Chrysler is recalling 2026 Ram 1500 vehicles because side air bag connectors may not be secured properly, potentially preventing deployment in a crash.
Chrysler is recalling 2026 Ram 1500 vehicles because tire pressure sensors may fail to detect low pressure or illuminate the warning light, increasing crash risk.
Nova Bus is recalling 2022-2023 LFS transit buses because short mounting screws may cause the bike rack to detach, creating a road hazard.
Chrysler is recalling 2022-2026 Ram Promaster and 2024-2026 Ram 3500 Electric vehicles because water may enter the steering wiring harness, potentially disabling power steering assist.
Mack Trucks is recalling 850 Anthem and Pioneer vehicles due to software errors that may reduce braking performance when hauling tanker trailers.
Volvo Trucks North America is recalling 2025-2027 VNL and 2026-2027 VNR trucks with tanker packages due to inaccurate axle load calculations that may reduce braking performance.
Cummins is recalling L9 diesel engines because remote fuel filter hoses may separate, causing fuel leaks, engine stalls, and increased fire or crash risks.