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.
Jerr-Dan is recalling 2009-2012 50 Ton Heavy-Duty Wreckers because mounting hardware may become loose or fracture, increasing crash risk.
Harsco Rail is recalling specific HY-RAIL rear guide wheel units installed on work trucks due to a potentially insufficient weld on the upper structure.
Norco is recalling 2011 Havoc 24-inch and 26-inch bicycles because the frame can crack at the top and down tube joint, posing a risk of injury or death.
Wilier Triestina is recalling Izoard XP bicycles because the fork's steerer tube can break, posing a fall hazard. No injuries have been reported.
Baby Jogger is recalling City Versa strollers because the frame can fail to lock and collapse, posing a fall hazard to children.
Porsche is recalling 455 model year 2010 911 GT3 vehicles because the rear wheel hubs may fail, potentially causing a loss of vehicle control and increasing crash risk.
Medtec is recalling 977 model year 2009-2011 ambulances because bench top screws may loosen and pull out, causing the bench top to drop and increasing the risk of personal injury.
NuVasive Inc is recalling 240 units of 6.5mm x 40mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
NuVasive Inc is recalling 240 units of 6.5mm x 55mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
NuVasive Inc is recalling 240 units of 4.5mm x 40mm Noncannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
NuVasive Inc is recalling 240 units of 7.5mm x 35mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
NuVasive Inc is recalling 240 units of 5.5mm x 45mm Noncannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
NuVasive Inc is recalling 240 units of 5.5mm x 45mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
NuVasive Inc is recalling 240 units of 5.5mm x 30mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
NuVasive Inc is recalling 240 units of 4.5mm x 35mm Noncannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
NuVasive Inc is recalling 240 units of 5.5mm x 50mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Stryker Spine is recalling 19 Mantis Torque Wrenches because the hex tip may fracture during use. The recall covers units distributed in the US and internationally.
Stryker Spine is recalling 28 units of Specialty Audible Torque Wrenches because the hex tips have fractured during use.
Captiva Spine is recalling 10 units of the CapLOX II Final Torque Driver because the device may break prematurely during use.
PACCAR is recalling specific TRP aluminum wheels because rim markings are etched too shallowly, failing federal safety standards and increasing crash risk.
Stryker Howmedica Osteonics is recalling 301 units of Peri-Acetabular Prosthesis V40 Femoral Extension Components due to insufficient taper torsional strength when used with forged CoCr stems.
Stryker Howmedica Osteonics Corp. is recalling 165 Hoffman LRF Telescopic Struts because three complaints reported the devices breaking during load-bearing use in patients weighing over 250 lbs.
Primus Medical LLC is recalling 342 Prime Bed TL500 hospital beds because retaining washers and clevis pins may fail, causing the bed frame to collapse.
Bike Friday is recalling Tikit folding bicycles because the handlebar stem can break, causing the rider to lose control and fall.
LaJobi is recalling Graco-branded Avalon and CNS Box 2 glider rockers because the base can crack or break, posing a fall hazard. Consumers should stop using the products and contact LaJobi for a free replacement base.