The Recall Desk

Hazard

Electrical Hazard recalls

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

What the numbers show

Total
80
Critical
0
Severe
10
Most recent
2026-06-10

Of the 80 electrical hazard recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 10 (13%) 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 hazard 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.

76–80 of 80

  • ModerateFDA (Devices)·Z-1615-2015·2015-05-20

    Siemens Dimension Chemistry Systems Recalled for Non-Standard Power Plugs

    Siemens Healthcare Diagnostics is recalling certain Dimension Integrated Chemistry Systems installed with non-standard power plugs due to a potential electrical hazard.

    Product
    Dimension EXL with LM, Dimension EXL 200, Dimension RxL, Dimension RxL HM, Dimension RxL Max, Dimension RxL Max HM, Dimension Xpand, Dimension Xpand HM, Dimension Xpand Plus, Dimension Xpand Plus HM. The Dimension EXL clinical chemistry system is a discrete, random-access
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0119-2015·2014-10-29

    Aerogen Recalls FRIWO Power Adapters for Aeroneb Nebulizer Systems

    Aerogen is recalling FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover may break and dislodge before use.

    Product
    The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb Professiona
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0994-2014·2014-02-26

    Integra CUSA Excel CEM Nosecone Recalled for Sticking Button

    Integra LifeSciences is recalling CUSA Excel CEM nosecones because the blue COAG button may stick in the activated position.

    Product
    Integra Cusa Excel Rx Only CEM" Nosecone for CUSA¿ Excel System Product Usage: Intended for use CUSA Excel/CUSA Excel + Ultrasonic Surgical Aspiration System, CUSA handpiece, and Covidien Force FX Electrosurgical Generator The CUSA Electrosurgical Module (CEM) provides De
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1941-2012·2012-07-11

    Pride Mobility Victory 9 Wheelchair Recalled for Harness Sealing Defect

    Pride Mobility is recalling 186 Victory 9 motorized wheelchairs because the main harness connector lacks required back shield sealing, allowing water to seep through.

    Product
    Victory 9 with Power Seat (SC609PS) Motorized wheelchair with elevating seat.
    Category
    Medical Device
    Distribution
    0 states