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.
Xootr is recalling about 3,000 adult kick scooters because the steer support can break during normal use, posing a fall hazard.
Rexon is recalling Black+Decker portable table saws sold at Walmart because the stand can collapse, posing laceration and impact injury risks.
Motor Coach Industries is recalling 2014-2016 J4500 vehicles because the front sway bar may crack and detach, increasing crash risk.
Haibike is recalling specific XDURO electric bicycles because the front fork can rupture or break, posing a fall hazard to riders.
Medtronic is recalling 1,096 units of BNX Fine Needle Aspiration Systems because the handle may break during use.
Medtronic is recalling SharkCore Fine Needle Biopsy Systems because the handle may break during use. The recall covers 1,096 units distributed in the US and two countries.
Medtronic is recalling 1,096 BNX Fine Needle Aspiration Systems because the handle may break during use.
Medtronic is recalling SharkCore Fine Needle Biopsy Systems because the handle may break during use, posing a risk of injury to patients or providers.
Medtronic is recalling SharkCore LG Fine Needle Biopsy Systems because the handle may break during use.
Trail King is recalling 2016-2017 ACS and AACS drop deck fifth wheel trailers because the coupler plate may crack, allowing the trailer to detach from the tractor.
Siemens is recalling 35 PRIMUS HI and Mevatron M2 linear accelerators due to a defective weld seam that could cause overhead suspensions to fall and injure people.
Prism Medical is recalling 76 A625 patient lifts because two units had straps break prematurely during internal testing at maximum load.
ErgoSafe Products is recalling 21 Prism Medical A625 manual lifts because two units had straps break prematurely during internal testing at maximum load.
Pier 1 Imports is recalling Neely and Dahlia bistro chairs because loose bolts can cause the legs to collapse, posing a fall hazard.
Rexon is recalling about 46,000 Craftsman portable table saws sold at Sears because the stand can collapse, posing laceration and impact injury risks.
L.L. Bean is recalling Adventure Adjustable Snowshoes because the plastic deck can weaken and break, posing a fall hazard. No injuries have been reported.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
New Flyer is recalling 2,357 transit buses from 2005-2007 because front axle beams may crack and fail, risking loss of vehicle control.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System trial trays due to potential alumina inclusions that could cause cracking and separation.
Biomet U.K. is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet U.K., Ltd. is recalling Oxford Knee System Tibial Resector Body Tubes and Guides due to potential alumina inclusions that could cause the instruments to crack or separate.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.