Hazard
172 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 172 equipment failure recalls we have scored against our rubric, 2 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 22 (13%) 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 equipment failure 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.
O'Brien Watersports is recalling Performer Pro Combo water skis because the bindings can detach during falls, causing the skis to break and injure users.
Shearwater is recalling yellow diving pressure transmitters because they may fail to signal tank pressure, posing a drowning hazard to divers.
Siemens is recalling 64 Artis Zee and Zeego angiography systems due to a possible cooling hose leak that can cause the X-ray tube to overheat and block imaging.
A M Systems Inc is recalling 610 units of Disposable Smooth Interior Tubing because the tubing may pull apart when stretched.
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 2,803 Bronchovideoscope BF-1T60 units because using non-Olympus accessories may loosen the instrument channel port.
Olympus is recalling 5,810 Bronchovideoscope BF-1T180 units because non-Olympus accessories may cause the instrument channel port to loosen.
Olympus is recalling 3,317 Bronchofiberscope F-1T160 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 3,041 Bronchovideoscope BF-1T40 units because using non-Olympus accessories may loosen the instrument channel port.
Olympus is recalling 861 Bronchovideoscope BF-XT160 units because using non-Olympus accessories may have caused the instrument channel port to loosen.
Hitachi is recalling one Scenaria CT system in Texas because the patient table failed to stop and contacted the gantry, posing a risk of injury.
Siemens is recalling 22 AXIOM Artis angiographic x-ray systems because leaking coolant couplings can damage the flat panel detector, potentially requiring treatment cancellation or patient transfer.
Halcore Group is recalling 2017 AEV Traumahawk ambulances because a battery isolator module may overheat, posing a fire and injury risk.
E-One is recalling 298 fire-fighting vehicles because corroding rings may cause pressure relief valves to open, reducing water pressure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that could cause equipment failure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that could cause equipment failure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that could cause equipment failure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that can cause equipment failure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems due to a cooling system leak that could cause equipment failure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that can cause equipment failure.
Siemens Medical Solutions is recalling 986 AXIOM Artis zee and Q angiography systems in the US due to a cooling system leak that could cause equipment failure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen x-ray systems in the US because a cooling system leak could cause equipment failure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US because a cooling system leak could cause equipment failure.
Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that can cause equipment failure.