Hazard
325 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 325 electrical shock recalls we have scored against our rubric, 2 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 58 (18%) 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 electrical shock 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.
Ketra is recalling about 3,400 D3 recessed downlights because incorrect wiring in the power supply connectors poses an electrical shock hazard. No injuries have been reported.
Altec is recalling 2016-2017 Aerial Devices and Digger Derricks because improperly sized cable connection receptacles may cause the high voltage grounding system to fail, increasing the risk of injury.
Schneider Electric is recalling Square D safety switches because power may remain on when the handle is in the OFF position, posing an electrical shock hazard.
Inova Diagnostics is recalling one QUANTA-Lyser 240 EIA instrument because a defective power supply may cause loss of protective grounding.
Inova Diagnostics is recalling one QUANTA-Lyser 240 IFA instrument because its power supply was not manufactured to specification, potentially causing loss of protective grounding.
Medtronic is recalling 449 O-arm O2 Imaging Systems because servicing internal components may cause an electrical short, posing a shock hazard to field service technicians.
Hitachi Medical Systems America Inc is recalling 55 ultrasound transducers (Model UST-5550-R) because they may not have adequate protection against electrical shock hazards.
Philips is recalling 10 CombiDiagnost R90 X-ray systems because a protective earthing wire was removed and non-standard spacers were used.
Skip Hop is recalling about 130,000 Moonlight & Melodies nightlight soothers because the USB wall power adapter can break, posing an electrical shock hazard.
Boston Scientific is recalling approximately 9,200 Emblem MRI S-ICD devices because memory corruption may cause the device to deliver an atypical amount of energy.
Pentax Medical is recalling 241 laryngeal strobe systems because isolation transformers were not always provided, posing a potential electrical safety risk.
R & D Products is recalling Outxpro mosquito zapper LED bulbs because the base can separate, posing an electrical shock hazard. No injuries have been reported.
Starcraft RV is recalling 2018 Launch Outfitter travel trailers because an electrical outlet lacks Ground Fault Circuit Interrupter protection, increasing the risk of electrical shock.
Nidec Motor Corp. is recalling about 16,000 swimming pool motors because the pump control cover can be improperly grounded, posing an electrical shock hazard.
Terex is recalling 2007-2016 aerial devices and digger derricks because the onboard electrical breaker may fail to trip during a short circuit, increasing the risk of user injury.
Goodman is recalling about 4,100 gas-fired furnaces because the blower motor is not grounded, posing an electrical shock hazard to individuals servicing the units.
SolarWorld is recalling about 97,000 solar panel connectors sold in the U.S. because microscopic cracks can allow moisture to leak in, posing an electrical shock hazard.
ASTI is recalling power adapters sold with LectroFan sound machines because the casing can break, exposing metal prongs and posing an electrical shock hazard.
Goodman is recalling approximately 210,000 air handler units because the pull-out disconnects may fail to disable power, posing an electrical shock hazard to individuals servicing the equipment.
Technical Consumer Products is recalling about 39,000 LED lamps sold at Habitat for Humanity in California due to an electrical shock hazard.
Siemens is recalling 762 SOMATOM CT systems because loose light marker windows could allow access to rotating or electrical parts.
Siemens is recalling SOMATOM Definition AS and Flash CT systems because light marker windows may become loose or drop out, creating a risk of contact with rotating or electrical parts.
Siemens is recalling 57 SOMATOM Definition Flash CT systems in the US due to a hardware issue that may expose users to rotating or electrical parts.
Siemens Medical Solutions is recalling 57 SOMATOM Definition AS CT systems due to a hardware issue that may expose users to rotating or electrical parts.
Forest River is recalling 2017 Vibe trailers because the kitchen stove may be connected to a live electrical circuit, posing a shock hazard.