Hazard
2,074 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 2,074 structural failure recalls we have scored against our rubric, 11 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,064 (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.
Alliance Outdoor Products is recalling about 3,400 climbing treestands because cable assemblies can separate due to corrosion, posing a fall hazard.
Vascular Solutions, Inc. is recalling 1,680 Langston Dual Lumen Catheters because the inner lumen may separate from the hub during pressure injection.
Olympus is recalling CHF-CB30S choledoscopes because they lack FDA clearance and have experienced breakage and metal protrusion during use.
Handicare AB is recalling SwiftHook components used in mobile and ceiling lifts because the carry bar may detach during use, posing a risk of injury to patients and caregivers.
Peloton is recalling PR70P clip-in pedals fitted on bikes sold between July 2013 and May 2016 because they can break unexpectedly, causing laceration injuries.
The Toro Company is recalling 2017-2020 model 22618 and 22618HD Log Splitters because tow pole mounting plates could bend, causing bolts to break and increasing crash risk.
Lamborghini is recalling 2020 Aventador SVJ Coupe and Roadster vehicles because loose front suspension anchor bolts may cause a loss of vehicle control.
Stoughton is recalling 2016-2019 DVW trailers because the rear suspension sub-frame may crack, causing hangers to detach and increasing crash risk.
Altec is recalling 280 units of 2019-2020 aerial devices and digger derricks because bolts securing the pedestal to the turntable may fail, posing a risk of injury or death.
Ford is recalling certain replacement brake pedal brackets that may fracture during sudden stopping, potentially affecting braking ability and increasing crash risk.
Braxton Creek is recalling 2020-2021 Bushwhacker travel trailers because undersized lag bolts may allow the floor to separate from the frame, increasing crash risk.
Genie is recalling 2020 TZ-50 trailers because bolted joints on the tongue structure may loosen and separate, increasing crash risk.
Jayco is recalling specific 2016-2019 motorhomes because leveling system brackets may fail, causing components to contact the ground and increasing crash risk.
Equipment Technology is recalling 2020 ETI ETC 37 IH aerial lift trucks because improper welds and steel thickness may cause the platform to fall unexpectedly.
American Hauler is recalling 2018 Air-Lite, Arrow, Falcon/XC, and Night Hawk trailers because spindle weld failures on the axles may increase the risk of a crash or injury.
Teleflex Medical is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The recall covers 20,600 units distributed nationwide.
Hill-Rom is recalling 1,033 Centralia Smart+ Beds because screws may not meet tensile strength requirements, posing a risk of serious injury.
Hill-Rom is recalling 257 Progressa Beds because screws may not meet tensile strength requirements, posing a risk of serious injury to patients or users.
OrthoPediatrics Corp is recalling 73 units of 6.0MM spine rods because incorrect laser etching may compromise strength and lead to unintended fracture.
Teleflex Medical Inc is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The devices are used for tracheal intubation.
Teleflex Medical Inc. is recalling 7,401 Rusch Greenlite laryngoscopes because the welded joint may break during use.
Teleflex Medical is recalling Rusch Greenlite laryngoscopes because the welded joints may break. The devices are used for tracheal intubation.
Teleflex Medical Inc is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The recall covers 27,341 units distributed nationwide.
Teleflex Medical Inc. is recalling 29,740 Rusch Greenlite laryngoscopes because the welded joint may break. The devices are used for tracheal intubation.
Walmart is recalling specific Hyper Tough 2 Ton Jack Stands that may collapse unexpectedly under load, posing a risk of injury to nearby persons.