Hazard
2,094 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 2,094 structural defect recalls we have scored against our rubric, 3 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,081 (52%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all structural defect 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.
Jaguar Land Rover is recalling 2016-2017 Discovery Sport and Range Rover Evoque vehicles because front lower control arm fasteners may fail, potentially causing the steering knuckle to separate.
Ford is recalling 2017 Fusion vehicles because improperly welded left rear seat back pivot pins may fail in a crash, allowing luggage to move into the passenger compartment.
Mitsubishi is recalling 2011-2012 and 2016 Outlander Sport vehicles because the lift gate support tube may corrode, causing the gate to fall suddenly and increase injury risk.
Autocar is recalling 2012-2016 Xpeditor vehicles because hybrid power drive unit bolts may not be tightened properly, risking detachment and crashes.
Bentley is recalling 378 model year 2017 Bentayga vehicles because seat mechanism and instrument panel joints may not have been properly tightened, increasing injury risk in a crash.
Hill-Rom is recalling 188 ceiling brackets with a larger center hole that could cause the system to fall if the safe working load is exceeded.
Terex Advance is recalling 2016-2017 Front Discharge Concrete Mixers because a front axle king-pin may fracture, potentially causing wheel separation and loss of vehicle control.
Nova Medical is recalling 1,380 Journey Rolling Walkers because screws holding the side supports can loosen and fall out.
Winnebago is recalling 2017 View and Navion motorhomes because loose seat mounting bolts may allow seats to detach, increasing injury risk.
Con-Tech is recalling 2015-2017 BridgeKing concrete mixer trucks because fender mounts may crack, causing fenders to detach and create road hazards.
X Spine Systems is recalling 195 units of Calix T PEEK Lumbar System TLIF Rasps because the tools may detach and become lodged in the surgical site.
Atwood Mobile Products is recalling specific left side seat adjusters used in vehicle seat belts because they may allow seats to move during a crash, increasing injury risk.
Ivolution Sports is recalling specific JX-SKY helmets because a metal screw prevents a detachable feature from releasing during a crash, increasing neck injury risk.
Jayco is recalling specific 2017 Eagle fifth wheel trailers due to axles with insufficient load capacity, which may lead to tire failure and increased crash risk.
Kaufman is recalling 2015-2016 Mini Car Haulers because a spring eye may break, allowing the axle to slide and potentially causing a crash.
Forest River is recalling 2017 Cedar Creek trailers because axles were misidentified as having a 7,000-pound capacity when they are only rated for 6,000 pounds.
Cardinal Health 200, LLC is recalling V. Mueller Neuro/Spine Shadow-Line Spinal Distraction Screws because corrosion was demonstrated on the screw surface.
Natus Medical is recalling 104 Medix NatalCare LX Intensive Care Incubators because a defective base weld may cause wheels to bend out of alignment.
Winco Mfg., LLC is recalling 264 TMM3 Series Video-Fluoroscopy Stretcher-Chairs because a non-conforming component caused the arms to no longer meet design specifications.
Winco Mfg. is recalling 264 TMM5 Series Mobile Surgical Stretcher-Chairs because non-conforming components caused the arms to no longer meet design specifications.
Winco Mfg. is recalling 264 TMM4 Series Multi-Purpose Treatment Chairs because a non-conforming component caused the arms to no longer meet design specifications.
Trumpf Medical Systems is recalling 84 TruSystem mobile operating columns because they may unexpectedly descend approximately 20 centimeters.
Argon Medical Devices is recalling 200 units of MicroStic Plus sheaths because the dilator hub is too small to secure the dilator to the sheath.
REV Ambulance Group is recalling 39 ambulances from 2016-2017 because defective seat tracks may allow attendant seats to move rapidly during a crash, increasing injury risk.
Subaru is recalling 2017 Legacy and Outback vehicles because the knee guard bracket may not be properly attached, increasing injury risk in crashes.