The Recall Desk

Hazard

Incorrect Wiring recalls

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

What the numbers show

Total
3
Critical
0
Severe
1
Most recent
2026-05-29

Of the 3 incorrect wiring recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (33%) 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 incorrect wiring 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.

1–3 of 3

  • HighNHTSA·26V352000·2026-05-29

    Forest River travel trailer fireplace outlets may have incorrect wiring

    Forest River is recalling certain 2024-2026 Wildwood and Salem travel trailers because the fireplace outlet may have incorrect wiring, increasing the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER STEALTH EVO, SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V477000·2022-07-06

    Travel Trailer Brake System Wiring Defect in Forest River Aurora

    Forest River Aurora travel trailers (2021-2022) have a brake system defect where the breakaway switch may be incorrectly wired, preventing trailer brakes from activating. Dealers will provide free inspection and repairs.

    Product
    COACHMEN — COACHMEN, FOREST RIVER CATALINA, AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3029-2017·2017-08-23

    GE Medical Systems Recalls Signa PET/MR Systems Due to Shock Hazard

    GE Medical Systems is recalling 68 Signa PET/MR systems because possible incorrect wiring of the Uninterruptable Power Supply could contribute to a potential shock hazard.

    Product
    Signa PET/MR (K163619, K142098) Product Usage: The SIGNA PET/MR system combines magnetic resonance diagnostic devices (MRDD) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information, acquired
    Category
    Medical Device
    Distribution
    Distributed nationwide