Hazard
86 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 86 non compliance recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 4 (5%) 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 non compliance 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.
5Color is recalling children's bike helmet and pads sets because the helmets violate mandatory safety standards, posing a risk of serious injury or death.
Victgoal is recalling about 40 children's bike helmets because they violate mandatory safety standards, posing a risk of serious injury or death from head injury.
Denago EV is recalling 2024-2026 electric vehicles that may fail to emit pedestrian warning sounds, increasing the risk of crashes.
Daimler Vans USA is recalling 2025 Mercedes-Benz eSprinter vehicles because they fail to make sufficient pedestrian warning sounds when in reverse, increasing injury risk.
Bell Sports is recalling Scout Air helmets in sizes S and L because they may lack proper penetration protection, failing federal safety standards.
Micro DOT Helmet Co. is recalling Blister and Twister helmets because they may lack proper penetration protection, increasing injury risk in crashes.
Chicco is recalling specific MyFit Zip Air Harness and Booster child seats because they may allow excessive chest movement in a crash, increasing injury risk.
Kido Sports is recalling Scorpion EXO Covert X and Harley-Davidson HD-X07 helmets because they may not stay securely fastened, increasing injury risk.
Jiangsu Shenli Medical is recalling 777,400 Wolf Medical 3 mL syringes (Model SYR03L) manufactured outside FDA clearance scope. Users should discontinue use of affected lot codes.
Nexxpro is recalling NEXX X.G10 helmets in sizes M and S because they may lack a required carbon layer, failing to provide adequate protection in a crash.
Entrans is recalling 2023 Polar Tank SCX9 trailers that may lack a rear impact guard certification plate, failing federal safety standards.
Comoto Holdings is recalling specific Bilt Route motorcycle helmets because they may lack adequate penetration protection, increasing injury risk during crashes.
Comoto Holdings is recalling specific Bilt Vertex motorcycle helmets because they may lack proper retention and penetration protection, increasing crash injury risk.
Comoto is recalling specific Bilt Grommet Youth helmets that may not adequately protect the wearer during a crash.
Prevost is recalling 2021-2023 X3-45 Commuter motorcoaches because the driver's seat has a Type 1 seat belt instead of the required Type 2, which may not adequately protect the driver in a crash.
Shyft Group is recalling 2021-2022 Utilimaster Walk-In Vans because the passenger-side jump seat headrest may be installed incorrectly, increasing injury risk in a crash.
Milwaukee Performance Helmets is recalling specific models that fail to meet federal safety standards due to potential defects in retention, protection, and labeling.
Great Dane is recalling 2019 Freedom Platform trailers that may lack rear impact guard certification plates, potentially affecting safety compliance.
Midwest Motorsports is recalling Kylin K77 helmets in sizes L, XL, and XXL because they may not adequately protect the wearer in a crash.
Nexxpro is recalling specific X.R2 motorcycle helmets because they may not adequately protect the wearer in a crash. Owners will receive free replacements.
Autoliv is recalling certain Automatic Locking Retractor (ALR) seat belt assemblies that may deactivate early. This defect increases the risk of injury during a crash.
Welch Allyn Inc Mortara is recalling 27 ELI 380 Electrocardiographs because they do not meet IEC 60601-2-27 requirements as labeled.
Barco N.V. is recalling MDNC-3421 diagnostic radiology displays because they were shipped without being DICOM-compliant. These units will not pass required acceptance tests.
SenTec AG is recalling 15 SenTec Digital Monitors because they require an isolation transformer in home care settings to meet safety standards.
Maquet Cardiovascular is recalling 51 Blood Monitoring Units (BMU 40) because the printed circuit boards do not meet IEC electrical safety standards for creepage distance.