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 two DigitalDiagnost 4 Flex units because a defective hook allows the footplate to fall, posing an injury risk to patients or operators.
Philips is recalling DigitalDiagnost Release 3 units because a defective hook may allow the footplate to fall or swing, posing an injury risk to patients or operators.
Philips is recalling DigitalDiagnost 4 Flex and Value units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Richard Wolf GmbH is recalling 12 units of Artholine Punch B 4, 6MM H 1, 6MM because a potential burr in the joint may increase the risk of injury when the device is opened.
Philips is recalling CombiDiagnost R90 units because a defective hook may allow the footplate to fall, posing an injury risk to patients or operators.
Philips is recalling DigitalDiagnost 4 Chest units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Becton Dickinson is recalling BD BBL GC-Lect Agar plates because some were made with Gentamicin instead of Vancomycin, which may cause false negative gonorrhea test results.
GE Healthcare is recalling Optima CT660 systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Elekta is recalling 2,998 Digital Accelerators worldwide due to a potential for uncontrolled extension of iViewGT or XVI detector arms.
Philips is recalling DigitalDiagnost Dual Detector units because the footplate hook may fail, causing the plate to fall and injure patients or operators.
Philips is recalling DigitalDiagnost 4.1 Flex and Value units because the footplate hook may fail, causing the footplate to fall and injure patients or operators.
GE Healthcare is recalling specific CT systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Hitachi is recalling one Scenaria CT system in Texas because the patient table failed to stop and contacted the gantry, posing a risk of injury.
Philips is recalling DigitalDiagnost Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Liebel-Flarsheim is recalling 28 Direct Digital Imaging Systems due to a software issue causing significant discrepancies between display and dosimeter readings in pediatric modes.
Philips is recalling DigitalDiagnost 4.1 Chest X-Ray units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.
Philips is recalling EasyDiagnost Eleva DRF units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling DigitalDiagnost Dual Detector units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Philips is recalling EasyDiagnost Eleva DRF units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling DigitalDiagnost Release 3.1 units because a defective hook allows the footplate to fall or swing, posing an injury risk to operators or patients.
Philips is recalling two DigitalDiagnost 2.x Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to operators or patients.
TriMed Inc. is recalling 722 Ulnar Osteotomy Compression Plates because instrument holes are located on the wrong side of the plate.
Zimmer Biomet is recalling 247 connecting bolts made from incorrect material, which may decrease fatigue strength and lead to fracture.
GE Healthcare is recalling Optima CT540 systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Philips is recalling DigitalDiagnost Release 3.1 units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.