Hazard
283 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 283 death recalls we have scored against our rubric, 111 (39%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 152 (54%) 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 death 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.
Volkswagen is recalling 2015 Tiguan and Audi Q5 vehicles because seat-mounted air bag inflators may rupture in a crash, potentially causing serious injury or death.
Ford is recalling 2004-2006 Ranger vehicles because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
Takata is recalling specific driver-side frontal air bag inflators that may rupture during deployment, potentially causing serious injury or death to vehicle occupants.
Honda is recalling 2016 CR-V vehicles because the driver's air bag inflator housing may be defective, posing a risk of serious injury or death in a crash.
Bed Handles Inc. is recalling approximately 113,000 portable bed handles sold without safety retention straps. The recall follows reports of four deaths caused by entrapment in gaps between the handle and mattress.
Elite Biomedical Solutions LLC is recalling 346 Alaris Medley LVP Bezel Assemblies used in infusion pumps due to a risk of administering inappropriate fluid quantities.
Elite Biomedical Solutions LLC is recalling 609 Alaris Medley LVP Frame Membranes because the defect could allow fluid intrusion, potentially leading to injury or death.
Chrysler is recalling 2008-2010 Dodge Challengers because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
Yamaha is recalling about 200 SRViper snowmobiles because the brake line can contact the clutch, causing brake failure and posing a risk of injury or death.
Altec is recalling 2013-2015 AH125, HL125, and AH150 aerial devices because rotation bearing fasteners may fail, posing a risk of injury or death.
Honda is recalling specific 2001-2011 Honda and Acura vehicles because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
BMW is recalling specific 2002-2006 models because moisture can cause the driver's air bag inflator to rupture, potentially sending metal fragments into the cabin during a crash.
Chrysler is recalling specific 2004-2011 Dodge, Chrysler, and Mitsubishi vehicles because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
Takata is recalling specific frontal passenger air bag inflators for certain Honda and Mazda vehicles due to a risk of rupture during deployment.
Takata is recalling specific frontal driver air bag inflator modules that may rupture during deployment, potentially causing serious injury or death.
Takata is recalling PSPI-L passenger air bag inflators in specific Honda, Toyota, Pontiac, and Subaru models. The inflators may rupture in a crash, sending metal fragments into the vehicle.
Toyota is recalling 2004-2005 RAV4 vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of serious injury or death.
Altec is recalling 3,889 aerial devices because cylinder lugs may crack, causing unintended boom movement and injury risk.
Yamaha is recalling about 875 model year 2015 YZ250FFL and YZ250FFW competition off-road motorcycles because the engine can lock up during operation, causing a crash.
ConMed is recalling 174,610 Adult Radiotransparent Electrodes because design changes to Philips AED connections may cause therapy delays, risking patient death or serious injury.
ConMed is recalling 174,610 Adult Radiotransparent Electrodes because design changes to Philips AED connections may cause therapy delays, risking patient death or serious injury.
ConMed is recalling 174,610 pediatric radiotransparent electrodes because design changes to Philips AED connections may cause therapy delays, risking patient death or serious injury.
ConMed is recalling multifunction electrodes due to a design change that may prevent connection to Philips AEDs, potentially delaying therapy.
ConMed is recalling Pediatric R2 Multifunction Electrodes because design changes to the connection with Philips Heartstart devices may cause connection failures, potentially delaying therapy and leading to patient death or serious injury.
ConMed is recalling Adult Radiotransparent Electrodes because a design change in Philips AEDs may prevent connection, delaying therapy and risking patient death or serious injury.