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.
Outdoors RV is recalling 2019-2020 Trail Series MTN TRX 22TRX toyhauler travel trailers because incorrectly mounted axles may cause unsafe towing conditions.
Blue Bird is recalling 2019-2021 school buses because insufficient roof rivets may allow roof sheets to separate in a crash, increasing injury risk.
Daimler Trucks North America is recalling 2014-2020 Thomas Built school buses because specific seats may lack sufficient impact absorption, increasing injury risk in crashes.
SynTec Seating Solutions is recalling S3B and S3C Base Convertible school bus seats because they may lack sufficient impact absorption, increasing injury risk in crashes.
Daimler Trucks North America is recalling 618 school buses because loose torque converter fasteners could cause the vehicle to become disabled in traffic, increasing injury risk during evacuation.
FCA US is recalling 2011-2018 right-hand drive Jeep Wranglers because the driver's seat belt buckle strap may fracture, rendering the seat belt inoperable.
Heartland is recalling 2020 Milestone recreational trailers because missing wood backers may allow the upper bunk bed to fall, posing an injury risk.
Zimmer Biomet is recalling 49 units of Vanguard XP Tibial Tray 83 mm because the locking bar may not fully engage.
Zimmer Biomet is recalling 567 units of XP-CR Tibial Trays because the locking bar may not fully engage.
Zimmer Biomet is recalling 498 XP-CR Tibial Trays because the locking bar may not fully engage.
Zimmer Biomet is recalling 480 units of the XP-XP Tibial Tray because the locking bar may not fully engage.
Zimmer Biomet is recalling specific XP-XP Tibial Trays because the locking bar may not fully engage. The recall covers units distributed in the US and several international regions.
Zimmer Biomet is recalling 1,282 units of the XP-XP Tibial Tray because the locking bar may not fully engage.
Zimmer Biomet is recalling 369 units of the XP-CR Tibial Tray - Interlok 75mm because the locking bar may not fully engage.
Zimmer Biomet is recalling 78 units of XP-CR Tibial Trays because the locking bar may not fully engage.
Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vehicles because head restraint spring pins may be missing or improperly mounted, increasing injury risk in a crash.
Zimmer Biomet is recalling 454 units of XP-CR Tibial Trays because the locking bar may not fully engage.
Toyota is recalling 2020 Supra vehicles because the driver's seat belt guide loop mount may be improperly welded, which could compromise restraint in a crash.
Stryker Communications is recalling 52 Berchtold Chromophare Dual Monitor Carrier Arms or Dual Flat Panels because the mounts may have insufficient welds.
General Motors is recalling 2020 Buick Enclave and Chevrolet Traverse vehicles because a crack in the right-hand frame rail may reduce crash performance and increase injury risk.
Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Bard Peripheral Vascular Inc is recalling 135 units of Equistream Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Bard Peripheral Vascular Inc is recalling 104 units of GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Bard Peripheral Vascular Inc is recalling Equistream XK Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Bard Peripheral Vascular Inc is recalling 161 units of Equistream Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.