Hazard
2,114 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 2,114 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 1,157 (55%) 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.
Daimler Vans USA is recalling 2016 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vehicles because a driveshaft bracket may not be properly welded, posing a fire risk in a crash.
REV Recreation Group is recalling specific 2015-2017 American Coach and Holiday Rambler motorhomes because interior step supports may be inadequately secured, creating an injury risk.
Terumo is recalling Sarns Centrifugal Pumps because cracks in the housing can cause fluid leaks during cardiac procedures. No patient injuries have been reported.
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 3 instruments due to potential alumina inclusions that could cause cracking and separation.
Siemens is recalling 194 PRIMUS radiation therapy systems due to incorrect collimator position displays and improper weld seams at the overhead suspension.
Siemens is recalling 194 ONCOR radiation therapy systems in the US due to incorrect collimator position displays and improper weld seams.
Encore Medical is recalling 13 LIMA Modular Revision Hip Stems because they were inadvertently re-sterilized, which may compromise the integrity of the safety screw.
Siemens is recalling 194 ARTISTE MV radiation therapy systems due to incorrect collimator position displays and improper weld seams.
Isuzu is recalling 2015-2017 NPR HD, NPR XD, NQR, and NRR trucks because burrs on the frame crossmember may cause transmission mounting studs to break, increasing crash risk.
Britax is recalling B-Agile and BOB Motion strollers because a damaged receiver mount can cause car seats to fall, posing a hazard to infants.
Blue Bird is recalling 2015-2018 Vision school buses because battery box brackets may crack, causing the box to detach and become a road hazard.
Philips is recalling one Allura Xper FD10 X-ray system because production errors left screws loose, potentially causing the C-arm to rotate uncontrolled.
Highland Ridge RV is recalling 2016-2017 Open Range fifth-wheel vehicles because axle hangers may puncture the riser tube, causing axle misalignment and tire failure.
Philips is recalling two Allura Xper FD20/15 systems because production errors may cause C-arm screws to loosen, leading to uncontrolled rotation.
Philips is recalling two Allura Xper FD20 C-arm systems because production errors left screws loose, posing a risk of uncontrolled rotation.
Philips is recalling one Allura Xper FD20 unit because production errors left screws loose, which could cause the C-arm to rotate uncontrolled.
Krasnyi Oktyabr Inc. is recalling dry eviscerated salted bream fish found to be uneviscerated during FDA sampling. The product was distributed in New York and California.
Toyota is recalling 2016-2017 Tundra trucks with resin rear bumpers because the brackets may break if stepped on, posing an injury risk.
Walker is recalling 2014-2017 Food Grade Tank Trailers because weld joints on the underride guard may crack, potentially causing the guard to detach and become a road hazard.
Pratt Industries is recalling 126 units of 2014 DC432LS9 and DC432LS9HL ISO Tank Chassis because a defective axle spindle may cause the wheel end to separate, increasing crash risk.
Amendia, Inc. is recalling six Ceres-C Standalone Cervical Interbody devices because they are missing a tantalum market pin.
In2Bones is recalling 40 units of NEOVIEW locking screws due to dimensional non-conformity of the thread on the screw head. The recall covers units distributed in the US, France, and Switzerland.
REV Recreation Group is recalling specific Renegade RV motorhomes because seat belt anchorage hardware may pull out of the floor framing during a crash.
GE Healthcare is recalling RFX and other systems because aged CRT monitors may fall. This poses a risk of injury or property damage.
GE Healthcare is recalling ADVANTX LCA and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and internationally.