The Recall Desk

Hazard

Bodily Harm recalls

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

What the numbers show

Total
5
Critical
1
Severe
0
Most recent
2021-04-12

Of the 5 bodily harm recalls we have scored against our rubric, 1 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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 bodily harm 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.

1–5 of 5

  • CriticalCPSC·21108·2021-04-12

    Black Diamond Recalls PIEPS DSP Avalanche Transceivers Due to Signal Loss Risk

    Black Diamond is recalling PIEPS DSP avalanche transceivers because they may switch modes unexpectedly, preventing signal transmission. One death and one injury have been reported.

    Product
    PIEPS DSP Pro, DSP Pro Ice, and DSP Sport Avalanche Transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1691-2019·2019-06-05

    NeuroLogica Recalls Samsung GM85 Mobile Digital X-ray Imaging Systems

    NeuroLogica is recalling 288 Samsung GM85 Mobile Digital X-ray Imaging Systems due to a potential safety latch issue that could cause the arm to fall.

    Product
    Samsung GM85 Mobile Digital X-ray Imaging System Product Usage: The GM85 Digital X-ray imaging System is intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0768-2016·2016-02-17

    GE Healthcare Optima XR220amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 2,389 Optima XR220amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.

    Product
    GE Healthcare, Optima XR220amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0769-2016·2016-02-17

    GE Brivo XR285amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 126 Brivo XR285amx mobile radiographic systems worldwide because a safety latch mechanism may fail, posing a risk of bodily harm.

    Product
    GE Healthcare, Brivo XR285amx Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0770-2016·2016-02-17

    GE Healthcare Optima XR200amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 895 Optima XR200amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.

    Product
    GE Healthcare, Optima XR200amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states