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.
Daimler Trucks is recalling 2014-2018 Thomas Built Buses Saf-T-Liner EFX and HDX school buses because occupant seats may lack under-rail washers, reducing anchorage strength.
Daimler Trucks North America is recalling 2013-2018 Thomas Built Saf-T-Liner HDX school buses because seat lap belts may be anchored to the seat rather than the bus structure.
Temsa is recalling 2014-2017 TS45 motorcoaches because improper fasteners on the leveling valve linkage may loosen and detach, potentially damaging tires and increasing crash risk.
Savaria Concord Lifts is recalling 226 Stairfriend stair lifts due to poor quality welding on the seat post.
Gulf States Toyota is recalling 2016-2017 4Runners with TFORCE accessory packages because roof rack fasteners may be improperly tightened, posing a crash risk.
Keystone RV is recalling 2017 CrossRoads Volante trailers because the rear upper bunk may not be properly supported, posing a risk of injury if the bunk falls.
Elcam Medical, Inc. is recalling 810 units of Minimal Residual Volume Luer-activated Swabable-stockcock devices found to have punctures.
Ferno-Washington Inc is recalling 34 units of the PROFlexx Model 28Z Chair Cot because an incorrect nut was used during manufacturing.
Grand Design is recalling 2017-2018 Imagine travel trailers because slide room screws may shear, allowing the room to extend while towing and increasing crash risk.
Stryker is recalling 292 Visum LED Surgical Lighting systems because missing screws and user overloading may cause the equipment to fall.
Hitachi Aloka Medical is recalling Prosound F75 ultrasound systems because the monitor arm may loosen. Affected units were distributed to specific US states.
Forest River is recalling 2016-2018 XLR Toyhaulers because weak fasteners may allow the side patio deck to drop unexpectedly, increasing crash risk.
Medtronic is recalling Poly Component Trial knee implants because the dovetails were observed as cracked or broken.
Medtronic Sofamor Danek USA Inc is recalling 72 units of Poly Component Trial knee implants because the dovetails were observed as cracked or broken.
Medtronic is recalling 111 units of Poly Component Trials because the dovetails were observed as cracked or broken.
Medtronic is recalling 72 Poly Component Trial knee implants because their dovetails were observed as cracked or broken.
Ford is recalling 2017 Edge vehicles with Panoramic Vista Roofs due to an improperly welded windshield header that reduces lateral structural integrity.
Tiffin is recalling 2011-2016 Allegro Open Road motorhomes because the tow hitch may detach under heavy loading or hard braking, increasing crash risk.
Hickory Springs is recalling specific school bus seats because a loose nut may allow the shoulder belt D-ring to detach in a crash, increasing injury risk.
Villa Sistemi Medicali is recalling 65 Apollo multi-function x-ray systems because the footrest detached from the table, causing a patient to fall.
Siemens is recalling 35 linear accelerator systems due to defective weld seams that could cause overhead suspensions to fall, posing a risk of severe injury.
Siemens is recalling 35 MEVATRON M 7400/7440 linear accelerators because a defective weld seam could break, causing the overhead suspension to fall and potentially injure patients or others.
Villa Sistemi Medicali is recalling 65 Apollo EZ x-ray systems because the footrest detached from the table, causing a patient to fall.
Siemens is recalling 35 MEVATRON M 6730/6740 linear accelerators because defective weld seams on overhead suspensions could break and fall, posing a risk of severe injury.
Villa Sistemi Medicali is recalling 65 Apollo DRF x-ray systems because the footrest can detach, causing patients to fall from the table.