Hazard
2,114 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 2,114 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 1,157 (55%) 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.
Daimler Trucks North America is recalling 2019-2020 Thomas Built school buses because the roof escape hatch handle may break, hindering emergency egress.
Teleflex is recalling 20 units of Neonatal ConchaSmart Breathing Circuits due to reported cracks on swivel wye adaptors observed prior to use.
Daimler Trucks North America is recalling specific Thomas Built Buses because the roof escape hatch handle may break, preventing emergency exit.
MORryde is recalling certain Orbital and You Turn Rubber Pin Box Wedge Kits because incorrect bolt lengths may prevent proper tightening, increasing crash risk.
MORryde is recalling certain You Turn and Orbital Rotating Pin boxes because they may have shorter bolts than required, increasing the risk of a crash.
Rinovum Women's Health is recalling the Revive Reusable Bladder Support because the device may split or crack during its intended use life.
Baxter Healthcare is recalling Revaclear 400 dialyzers because ruptured fibers may cause blood leaks during hemodialysis treatment.
Winnebago is recalling 2017-2019 Forza motorhomes because the exterior storage compartment door may unexpectedly open while driving, increasing crash risk.
The FDA is recalling 3,113,280 units of the EGIA 60 Articulating Extra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious surgical complications.
Subaru is recalling 2019 Legacy and Outback vehicles because improperly applied spot welds may reduce body strength, increasing injury risk in a crash.
The FDA is recalling 3,113,280 units of the EGIA 30 Articulating Medical device due to missing pin components that may cause incomplete staple formation and serious surgical complications.
The FDA is recalling 3,113,280 units of the EGIA 45 Articulating Xtra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious medical complications.
Cook Inc. is recalling 73 Advance Enforcer 35 Focal Force PTA Balloon Catheters because they may burst below the rated pressure, posing risks of vessel injury and balloon fragmentation.
Charles Machine is recalling 2018-2019 Ditch Witch trailers because hitch lock nuts may fail to clamp the load, increasing crash risk.
Specialty Manufacturing is recalling Prolo 24-inch roof hatches because the external handle may break, preventing emergency exit from the vehicle.
Erwin Hymer is recalling 2013-2019 Roadtrek motorhomes because second-row seat anchor brackets may lack sufficient strength, increasing injury risk in a crash.
Porsche is recalling 2019 911 GT2 RS and 2020 911 Carrera S Coupe vehicles because driveshaft bolts may not be properly tightened, increasing crash risk.
Keystone is recalling 2020 Crossroads Cruiser fifth wheel trailers because the furnace exhaust vent may be missing, creating a carbon monoxide risk.
Ford is recalling 2011-2017 Explorers because rear suspension toe links may fracture, causing sudden handling changes and increasing crash risk.
Karma Automotive is recalling 295 2018 Karma Revero vehicles because the upper intrusion bar in the front left door may be split, reducing side-impact protection.
Seats Incorporated is recalling ABTS 6-way seats because poor weld penetration may cause the seat to move unexpectedly, increasing injury risk in a crash.
Stryker is recalling 3,176 EDS Light Suspension components for the Visum LED Surgical Lighting System due to a potential assembly defect in the joint.
CooperSurgical is recalling 480 ICSI Micropipettes because the required thirty-degree bend is absent. The affected units were distributed in Denmark, Italy, and Sweden.
Ethicon Endo-Surgery is recalling 434,614 Curved Intraluminal Staplers (Model CDH33A) because they may have an insufficient firing stroke to break the washer and form staples.
Entrans is recalling 2017-2020 Heil AJB9-1040 Hybrid trailers because frame cracks may develop, affecting handling and increasing crash risk.