Hazard
189 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mechanical failure recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
Certain 2025 Winnebago Spirit and Minnie Winnie motorhomes may have spare tire carrier mounting bolts that loosen, allowing the carrier to detach and become a road hazard. Dealers will replace and torque the bolts free of charge.
Philips Azurion 7M20 X-ray imaging systems may experience inconsistent or unavailable motorized movement on the ceiling-mounted FlexArm arm due to bearing lubrication failure affecting 172 units.
Shimadzu ceiling X-ray supports may have a defective shaft that could cause the tube assembly to detach. The FDA has recalled approximately 1,766 affected units.
GE HealthCare is recalling certain Myosight dual-head nuclear medicine gamma cameras that may have been transported without adequate detector support, potentially resulting in detector failure and serious bodily injury.
GE HealthCare recalled 205 Sopha Medical Vision dual-head gamma cameras that may have been transported without adequate support, creating detector fall risk and potential life-threatening injury.
GE HealthCare recalls Starcam/Camstar nuclear medicine gamma cameras that may have been transported without adequate detector support. Unsupported systems could experience detector falls, potentially causing life-threatening injury.
GE Medical Systems is recalling 64 Elscint Model 4XX nuclear medicine gamma cameras past their end of guaranteed service due to risk of detector fall from inadequate support during transport or relocation, which could cause life-threatening injury.
Cardinal Health is recalling Salem Sump Silicone Dual Lumen Stomach Tubes with Anti-Reflux Valve due to complaints of valve breakage from excessive force during use. The manufacturer is providing additional guidance for proper use.
Certain Elscint Varicam nuclear medicine gamma cameras may have been transported without adequate detector support, risking detector falls and life-threatening injury.
The Atlan A350 anesthesia workstation's piston ventilator may fail before use or during mechanical ventilation. FDA classified this Class I recall as affecting 530 units distributed across U.S. hospitals and internationally.
Philips CT systems' patient support table may unexpectedly descend to the lowest position due to ball screw misalignment after component replacement. No injuries have been reported. Affected healthcare facilities should contact Philips for guidance.
Philips is recalling CT systems whose patient support tables may descend unexpectedly due to ball screw misalignment. The recall affects 285 units distributed worldwide.
Philips CT systems (Model 728324) may have patient support tables that descend unexpectedly due to ball screw misalignment after replacement, posing a fall risk.
Philips is recalling 3 Ingenuity CT Family Brazil scanner units due to a potential defect where the patient support table may descend unexpectedly to the lowest position after ball screw replacement. No injuries have been reported.
Philips CT systems' patient support tables may descend unexpectedly to the lowest position due to ball screw misalignment after component replacement. This poses a fall risk to patients.
Philips IQon Spectral CT systems' patient support tables may descend unexpectedly to the lowermost position due to ball screw misalignment after component replacement.
Philips Brilliance iCT CT systems may have faulty patient support tables that descend unexpectedly due to component misalignment, creating a risk of patient injury.
Philips is recalling certain CT 6000 systems because the patient support table may descend unexpectedly to the lowest position due to ball screw misalignment after replacement, creating a fall risk.
Encore Medical is recalling 927 units of the ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD due to a potential for mechanical failure during surgical use, where the reamer may kick or bind. No injuries have been reported.
THOR Photomedicine recalls the NovoTHOR Gen 3.0 light therapy device due to faulty welded nuts that can shear off, detaching the gas strut and making the canopy difficult to lift.
GE HealthCare is recalling certain MR imaging systems because planned maintenance checks for patient table caster lock functionality may not have been performed, posing a potential safety risk.
Medtronic is recalling 3 units of the O-arm O2 Imaging System (mobile X-ray equipment) in IN, MN, and MS due to potential damage to a mechanical component supporting the gantry during manufacturing.
Kawasaki has recalled about 3,400 model year 2025 KX series motorcycles due to a primary gear defect that can fail and cause a crash. No injuries have been reported.
Stryker Spine has recalled 56 units of the Monterey AL Implant Inserter due to potential separation of the gold unlock button. This could impair the device's function during surgical implant placement.
Tyber Medical is recalling A.L.P.S. mvX Anatomic Lateral Fibula Plates nationwide due to reports that locking screws may pass through the locking hole during surgery, causing surgical delays.