The Recall Desk

Hazard

Electrical Shock recalls

325 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
325
Critical
2
Severe
58
Most recent
2026-08-26

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

About this hazard tag

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.

1–25 of 325

  • HighFDA (Devices)·Z-2983-2026·2026-08-26

    Fort Defiance Automated Field Steam Sterilizer Recalled for Electrical Grounding Defect

    Fort Defiance Industries is recalling Automated Field Steam Sterilizers because a water recovery system connector may lose ground continuity, creating an unreliable fault current return path.

    Product
    Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V426000·2026-07-02

    Jayco Recalls 2026 Seismic Fifth Wheel Toy Haulers Due to Fire Risk

    Jayco is recalling 2026 Seismic fifth wheel toy haulers because the inverter may lack a grounding connection, increasing the risk of fire and electrical shock.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26576·2026-06-25

    Lomi roll-on waxing kit power cords can overheat and short circuit

    About 14,700 Lomi Roll-On Waxing Kits are being recalled because the warmer's power cord can overheat and short circuit, posing fire, burn and shock hazards.

    Product
    Lomi Roll-On Waxing Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2314-2026·2026-06-17

    GE Allia IGS 3 Pulse systems pose shock risk to servicers

    Allia IGS 3 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. Nine units affected.

    Product
    Allia IGS 3 Pulse angiographic X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2315-2026·2026-06-17

    GE Allia IGS 5 Pulse systems pose shock risk to servicers

    Allia IGS 5 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. 121 units affected.

    Product
    Allia IGS 5 Pulse angiographic X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2318-2026·2026-06-17

    GE Allia Moveo angiographic systems pose shock risk to service personnel

    Allia Moveo angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. Three units affected.

    Product
    Allia Moveo angiographic X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2317-2026·2026-06-17

    GE Allia IGS Pulse systems pose shock risk to service personnel

    Allia IGS Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on.

    Product
    Allia IGS Pulse angiographic X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2316-2026·2026-06-17

    GE Allia IGS 7 Pulse systems pose shock risk to servicers

    Allia IGS 7 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. 35 units affected.

    Product
    Allia IGS 7 Pulse angiographic X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2282-2026·2026-06-10

    Neptune docking station shipped without verified electrical safety testing

    A Neptune Smart Docking Station is being recalled because it was not released from manufacturing and may not have completed required testing, leaving a potential shock risk.

    Product
    Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V226000·2026-04-09

    IC Bus Recalls EVSB School Buses Due to High Voltage Switch Defect

    International Motors is recalling 2022-2027 IC Bus EVSB school buses because a high voltage disconnect switch may fail to shut off power, posing a risk of electrical shock.

    Product
    IC BUS — IC BUS EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1894-2025·2025-06-11

    Signature Laparoscopic Allis Clamp Grasper with Rotating Shaft Recalled

    Silex Medical is recalling the Signature Laparoscopic Instruments Allis Clamp Grasper due to incomplete insulation on the shaft, leaving an exposed area that could pose an electrical hazard during surgical procedures.

    Product
    Signature Laparoscopic Instruments, Allis Clamp Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862030.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·25317·2025-06-05

    Lutron Power Interfaces for LED Tape Lights Recalled for Shock Hazard

    Lutron-branded power interfaces for LED tape lights can fail during power surges like lightning strikes, creating a shock hazard. About 1,944 units are affected; no injuries have been reported.

    Product
    Lutron-branded power interfaces for LED tape lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25211·2025-04-03

    LVOE Hair Dryers Recalled for Electrocution and Shock Hazards

    AliExpress is recalling LVOE-brand hair dryers sold from April 2023 through December 2024 because they lack immersion protection and can cause electrocution if they fall into water while plugged in. No injuries have been reported.

    Product
    LVOE Hair Dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25E001000·2025-01-13

    Nivion NSP01 Charger Adapter Recall for Electrical Arcing Risk

    N&B Mobility Solutions is recalling Nivion NSP01 charger adapters due to electrical arcing and shock risks. Owners should contact Nivion for a free replacement.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:CHARGING:CABLE/CORD:ACCESSORY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V959000·2024-12-20

    Gillig Recalls 2023-2024 Low Floor Buses Due to Electrical Interlock Defect

    Gillig is recalling 2023-2024 Low Floor transit buses because a high-voltage air compressor may not be connected to the safety interlock loop, increasing the risk of electrical shock.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V934000·2024-12-17

    Cummins Recalls 2022-2024 Trailer-Mounted Generators Due to Wiring Defect

    Cummins is recalling 2022-2024 C275D2RE trailer-mounted generators because unsecured wire leads may chafe and short circuit, increasing the risk of electrical shock or fire.

    Product
    CUMMINS POWER GENERATION — CUMMINS POWER GENERATION GENERATOR SET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0466-2025·2024-11-27

    Smiths Medical CADD-Solis AC adapter input plugs pose electrical shock risk

    Smiths Medical is recalling 156,400 CADD-Solis AC adapters due to damaged or broken input plugs that may expose metal contacts. The affected adapters could pose a risk of electrical shock or fire.

    Product
    smiths medical CADD-Solis Li-ion Rechargeable Battery Packs AC adapter, Model Number REF 21-0270-25, for use with the CADD-Solis infusion pumps
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0370-2025·2024-11-20

    Stryker Smoke Evacuation Pencils Recalled for Unintended Activation Risk

    Stryker is recalling 403,730 Neptune SafeAir Smoke Evacuation Pencil units because they may activate unexpectedly when plugged in, creating a risk of electrical burns to patients and physicians.

    Product
    Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button, Bulk Non-sterile - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuatio
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V800000·2024-10-24

    Orange EV Recalls T-Series and e-TRIEVER Trucks for Manual Errors

    Orange EV is recalling 2017-2024 T-Series and 2023-2024 e-TRIEVER trucks because manuals incorrectly describe the high-voltage lockout procedure, posing an electrical shock risk.

    Product
    ORANGE EV — ORANGE EV T-SERIES ELECTRIC TRUCK, E-TRIEVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0052-2025·2024-10-16

    Monarch Platform Urology Device Recalled for Power Cord Electrical Hazard

    Auris Health is recalling Monarch Platform (Urology) devices due to strain relief defects in power cords that may cause electrical short and potential shock to operating room staff.

    Product
    Monarch Platform (Urology), REF: MON-000007, MON-000007-RFB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0051-2025·2024-10-16

    Endoscopy and Bronchoscopy Systems Power Cord Defect Risk

    Monarch Platform endoscopy and bronchoscopy systems may have defective power cords causing electrical shorts and shock risk if exposed wires are touched, potentially leading to system shutdown.

    Product
    Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005-01R. Monarch Platform (Bronchoscopy), REF: MON-000006, MON-000006-RFB.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3080-2024·2024-10-02

    GE Giraffe Warmer Recalled for Incomplete Electrical Safety Testing

    Wipro GE Healthcare is recalling specific GE Giraffe Warmers because incomplete electrical safety testing during manufacturing may allow leakage current to exceed safety limits.

    Product
    GE Giraffe Warmer, Model/Catalog Number M1118179-01090979. Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Infant radiant warmers may be used to facilitate the neonate's transition t
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·24V663000·2024-09-10

    Alliance RV Valor travel trailers recalled for missing electrical shock protection

    Alliance RV is recalling certain 2024-2025 Valor travel trailers where the front bathroom outlet may lack Ground Fault Interrupter (GFI) protection. This missing safety feature can result in electrical shock.

    Product
    ALLIANCE RV — ALLIANCE RV VALOR
    Category
    Vehicle
    Distribution
    Distributed nationwide