Hazard
2,056 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 2,056 structural failure recalls we have scored against our rubric, 10 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,049 (51%) 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 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.
Siemens is recalling 73 Artis X-ray systems because ceiling-mounted support screws may loosen or snap, posing a risk of severe injury.
Siemens is recalling 63 Artis zee X-ray systems because ceiling support screws may loosen or snap, posing a risk of severe injury to patients and staff.
Siemens is recalling 29 Artis X-ray systems because ceiling mount screws may loosen or snap, posing a risk of severe injury to patients and staff.
Siemens is recalling 15 Artis X-ray systems because ceiling mount screws may loosen or snap, posing a risk of severe injury to patients and staff.
Altec is recalling 2018-2019 aerial devices because high-strength fasteners securing the pedestal to the turntable may fail, increasing the risk of injury or death.
SRAM is recalling RockShox Lyrik and Yari front suspension forks because the lower leg assembly can break, causing riders to lose control and crash.
Faraday is recalling about 4,450 electric bicycles because the seat posts can break, posing a fall hazard to riders.
Skytron is recalling five Integrity 270 Steam Sterilizers because the weld attaching the air heater assembly has shown signs of fatigue or failure.
GE Healthcare is recalling Precision 500D X-ray systems because a CRT monitor fell off its wall mount due to product aging.
GE Healthcare is recalling Prestige II, SI, and VH systems because a CRT monitor fell off its wall mount due to product aging.
Altec is recalling 2017-2018 aerial devices because fasteners securing the rotation bearing may break, potentially causing the pedestal to separate from the turntable.
Autocar is recalling 2013-2018 Xpeditor vehicles because the drive shaft support cross member may fail, increasing crash risk. Dealers will install additional support brackets free of charge.
OriGen Biomedical is recalling 66 units of ECMO Reinforced Dual Lumen Cannulas due to a risk of the clear tube disconnecting from the hub.
Lakota is recalling 2018-2020 Colt horse trailers because a weak aluminum axle carrier may tear, affecting stability and increasing crash risk.
Xtreme Outdoor Products is recalling climbing sticks that can break due to bolt failure, posing a fall hazard and risk of serious injury.
Audi is recalling 2019 A8 vehicles with rear relaxation seats because a front passenger seat track rivet may fail. This defect increases the risk of injury during a crash.
Keystone is recalling 2019-2020 Dutchmen Voltage 4185 trailers because an undersized fifth wheel pin box may fail under heavy loads, increasing crash risk.
Moller Vital is recalling 427 Molift 2-Point sling bars because broken hooks may cause the sling to slip, potentially leading to patient falls.
Stryker is recalling 3,285 Power-LOAD Cot Fastening Systems because the floor plates holding ambulance cot anchors may be broken.
R82 A/S is recalling 68 Wombat Living activity chairs (wheelchairs) in North Carolina due to reports of the plastic joint connecting the back to the seat breaking.
Spartan Motors is recalling 2004-2016 Gladiator aerial vehicles because cracks in the tiller frame may cause the device to fall, risking injury.
Smeal is recalling 2017-2019 Aerial Fire Apparatus vehicles because missing joint welds in the base rail may cause the aerial device to collapse.
FCA US is recalling 2018-2019 Ram 1500 trucks because an incomplete weld on the rear driveshaft may crack or fracture, creating a road hazard or loss of drive power.
Medrobotics is recalling 35 Flex Robotic System obturators because a weld may break, causing the rod to separate from the cone.
Medrobotics is recalling 24 Flex Robotic System obturators because a weld may break, causing the rod to separate from the cone.