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.
HME is recalling 2013-2021 AF1, 1871, and SFO vehicles because cracked wiring insulation may cause aerial controls to fail, creating a shock risk.
Certain 2021 Keystone Cougar trailers equipped with the Off the Grid Solar package may have an incorrectly wired inverter that energizes the shore power connection, posing an electrical shock risk. Keystone will repair the inverter at no charge.
Northern Tool & Equipment is recalling Powerhorse 13000ES portable generators due to a wiring error that can cause electrical shock. No injuries have been reported.
Carl Zeiss Meditec is recalling 132 VISUREF 150 diagnostic instruments due to an incorrect component that may cause electrical shocks to users.
Carl Zeiss Meditec is recalling VISULENS 550 refractive power measurement devices due to a defective communication board that may cause electrical shocks.
Certain 2020-2021 Keystone Cougar trailers with solar packages have incorrectly wired inverters that may energize shore power connections, creating a risk of electrical shock.
Fresenius Medical Care is recalling 15 AquaBplus water purification systems due to incorrectly crimped connectors that could cause electrical shock.
Foretravel is recalling 2020 iC-37 motorhomes with Xantrex inverters that have duplicate ground/neutral bonds, creating a risk of electrical shock.
Hercules is recalling Moravian Star lights because they lack adequate wire size and overcurrent protection, posing fire and electrical shock risks.
Keystone Fuzion and Impact toy hauler travel trailers may have incorrectly wired generator transfer switches that could energize the shore power connection, creating an electrical shock hazard. Keystone will inspect and correct the wiring at no charge.
Forest River is recalling specific 2021 Riverstone trailers equipped with an optional generator prep package due to incorrect transfer switch wiring that may cause voltage back feed.
Siemens is recalling 20 Cios Spin X-Ray systems because unplugging the monitor cable can create unsafe voltage, posing an electrical shock hazard.
Siemens is recalling 58 Cios Alpha X-Ray systems because unplugging the monitor cable can expose users to unsafe electrical voltage, posing a shock hazard.
Siemens is recalling four Cios Alpha mobile X-ray systems because unplugging the main cable during a clinical session can expose users to unsafe electrical voltage.
Siemens is recalling 16 Cios Alpha mobile X-ray systems because unplugging the main cable during a clinical session can expose users to unsafe electrical voltage and shock.
Siemens is recalling 46 Cios Spin mobile X-ray systems because unplugging the main cable during a clinical session can expose users to unsafe electrical voltage.
Leviton is recalling approximately 98,000 50-ampere electrical connectors, plugs, receptacles, and inlets sold in the US and Canada due to mislabeled terminal markings that pose an electrical shock hazard.
Stryker is recalling Strykeprobe Outer Sheath Replacements because a length mismatch could cause the probe to melt, compromising insulation and allowing electricity to flow to the patient.
Hawthorne Hydroponics is recalling approximately 60,000 Grower's Edge Vaporizers because they can overheat, causing burns, fires, or electrical shocks.
Carl Zeiss Meditec is recalling 151 PLEX Elite 9000 Swept-Source OCT devices because a design fault may expose operators to hazardous voltage when contacting the metal enclosure.
Skylight is recalling Series I power adapters sold with digital photo frames because the casing can break, exposing metal prongs and posing an electrical shock hazard.
GE Healthcare is recalling 43 CardioLab/ComboLab Recording Systems because a failure in connected devices could cause electrical shock to patients.
GN Otometrics is recalling 3,071 ICS CHARTR EP 200 units because undergrounded electrical surfaces may cause electrical shock to patients or healthcare professionals.
VIQUA is recalling solenoid valve kits for UV water treatment systems because electrical current could leak, posing a shock hazard. No injuries have been reported.
Forest River is recalling 2020 Cherokee trailers because missing protective paneling exposes distribution panel wiring, increasing the risk of electrical shock or fire.