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.
Olympus is recalling 1,347 Bronchofiberscope BF-40 units because attaching non-Olympus accessories may loosen the instrument channel port.
Olympus is recalling 1,461 Bronchovideoscope BF-XP160F units because using non-Olympus accessories may cause the instrument channel port to loosen.
Olympus is recalling 3,041 Bronchovideoscope BF-1T40 units because using non-Olympus accessories may loosen the instrument channel port.
Olympus is recalling 3,948 Bronchovideoscope BF-160 units because attaching non-Olympus accessories may loosen the instrument channel port.
Olympus is recalling 2,318 Bronchovideoscope BF-3C160 units because attaching non-Olympus accessories may have caused the instrument channel port to loosen.
Olympus is recalling 861 Bronchovideoscope BF-XT160 units because using non-Olympus accessories may have caused the instrument channel port to loosen.
Olympus is recalling 5,545 Bronchofiberscope BF-P60 units because attaching non-Olympus accessories may cause the instrument channel port to loosen.
Olympus is recalling 653 Bronchovideoscope BF-MP60 units because non-Olympus accessories may cause the instrument channel port to loosen.
Collins is recalling 2011-2018 school buses because seat foam may not absorb enough impact in a crash, increasing injury risk.
Bausch & Lomb is recalling Stellaris Elite 20 GA Vit Cutters because the back cap may separate from the body of the device.
Biomet UK Ltd. is recalling specific HipLOC hip fracture fixation system plates due to an undersized bore that prevents the lag screw from fitting.
Bausch & Lomb is recalling Stellaris Elite 23 GA Vit Cutters because the back cap may separate from the body of the device.
Bausch + Lomb is recalling Stellaris Elite Vit Cutters because the back cap can separate from the cutter body.
Bausch & Lomb is recalling Stellaris Elite Vit Cutters because the back cap may separate from the cutter body.
Bausch & Lomb is recalling Stellaris Elite Vit Cutters because the back cap may separate from the cutter body.
Bausch & Lomb is recalling Stellaris Elite 23 GA Vit Cutters because the back cap may separate from the cutter body.
Bausch & Lomb is recalling Stellaris Elite 23 GA Vit Cutters because the back cap may separate from the cutter body during use.
Jayco is recalling 2019 Precept and Precept Prestige motorhomes because improperly heat-treated front wheel studs may break, increasing crash risk.
Chrysler is recalling 2018-2019 Jeep Wranglers because improperly welded front track bar brackets may separate, reducing steering capability and increasing crash risk.
ShinChang Medical Co., Ltd. is recalling 6,570,800 disposable insulin syringes because a small crack was found in the top end of the barrel near the needle.
Exactech is recalling one unit of the Optetrak Logic CC Stem Extension because it may have non-conforming internal threads.
Lion Electric Company is recalling 2016 Lion C electric school buses because ceiling joints may separate in a crash, increasing injury risk.
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.