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.
Ford is recalling 2013 C-Max hybrid vehicles without panoramic roofs because they failed to meet federal head injury safety standards. Dealers will install energy absorbers to reduce injury risk in crashes.
SpineFrontier, Inc. is recalling InSpan Inserter assemblies because a set screw may become deformed. The recall covers 61 units distributed worldwide.
Mitsubishi is recalling 2013 Outlander Sport vehicles due to a defective front stabilizer link weld that may damage tires or brake hoses, increasing crash risk.
Thermo King is recalling Precedent S-600 transportation refrigeration units manufactured in April and May 2013 because the lifting bracket may break, posing a risk of injury if the unit falls.
EverGreen is recalling 2013 Bay Hill fifth wheel travel trailers because a design change may cause awning motor screws to shear, risking injury or crashes.
Baxter Healthcare is recalling Infusor SV and LV Elastomeric Infusion Devices due to an increase in rupture complaints. The recall aims to ensure no affected product remains in the field.
Maquet is recalling specific pediatric arterial cannula packs because they may contain incorrectly sized connectors. The recall affects 100 units distributed in the US and internationally.
Baxter Healthcare is recalling 3.2 million Basal/Bolus Infusors due to increased rupture complaints. The devices are used for intravenous medication administration.
Baxter Healthcare is recalling Intermate Infusion Pumps due to an increase in rupture complaints. The recall covers 3,255,096 units distributed nationwide and in Puerto Rico.
Chrysler is recalling 2013 RAM 4500 and 5500 trucks because an incorrect bolt may break, causing the vehicle to pull to one side and increasing crash risk.
La Boit is recalling 2013 Mobile Services vehicles because power awning motor screws may shear, causing the awning to unfurl unexpectedly and increasing crash risk.
Zimmer, Inc. is recalling 344 Patient Helper Bed Frame Adapter Assemblies because they may have a weak weld where the mounting bars attach to the tube.
Ohlins is recalling steering dampers for BMW motorcycles because an incorrectly machined bracket may crack, potentially causing steering to lock and leading to injury or a crash.
OrthoPediatrics Corp is recalling 90 Degree Cannulated Infant Blade Plates due to reports of the plates bending during surgery.
Tesla is recalling 1,228 2013 Model S vehicles because a weakened weld on the left second-row seat back may cause it to detach in a crash, increasing injury risk.
Temsa is recalling 256 motorcoaches because over-tightened seat belt bolts may fail in a crash, increasing injury risk.
Intuitive Surgical is recalling approximately 132,441 EndoWrist Monopolar Curved Scissors instruments worldwide. The recall addresses potential cracks that may cause electrosurgical energy leaks and thermal injury to tissue.
Hill-Rom, Inc. is recalling 8,737 Hill-Rom 1000 Beds because brakes may disengage when the bed frame is subjected to a hard jolt or force.
Cordis Corporation is recalling 23 units of FLEXSTENT Biliary Self-Expanding Stent Systems because holes or tears can form in the inner or outer pouches.
Cordis is recalling 1,357 FLEXSTENT Biliary Self-Expanding Stent Systems because holes or tears can form in the inner or outer pouches.
Shimadzu Medical Systems is recalling 200 Mobile DaRt Evolution X-ray systems due to a potential risk of internal screws becoming loose.
Cordis Corporation is recalling 310 FLEXSTENT stent systems because holes or tears can form in the protective pouches, potentially compromising the device.
Carl Zeiss Meditec is recalling six OPMI Pentero C surgical microscopes because broken screws were found in the ceiling mounts during routine inspections.
Combi USA is recalling specific child seats because the harness webbing fails to meet minimum breaking strength requirements, increasing injury risk in crashes.
Chrysler is recalling 5,622 model year 2012 Dodge Ram 4500 and 5500 trucks because a welding defect may cause the front drive shaft to fracture, potentially leading to a loss of motive power and increased crash risk.