The Recall Desk

Hazard

Compression Injury 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
0
Most recent
2015-01-14

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

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all compression injury 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

  • HighFDA (Devices)·Z-0913-2015·2015-01-14

    Siemens Symbia Intevo SPECT CT Systems Recalled for Detector Motion

    Siemens is recalling six Symbia Intevo SPECT CT systems worldwide because unintended detector motion may cause patient compression injuries.

    Product
    The Symbia Intevo Excel is a non-diagnostic SPECT ICT system with CT support for only attenuation correction and anatomical localization. The Symbia Intevo Series are xSPECT systems. These are SPECT and T systems integrated through xSPECT technology during image registration
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0911-2015·2015-01-14

    Siemens Symbia S Series Medical Imaging Systems Recalled for Detector Motion

    Siemens is recalling 877 Symbia S series imaging systems due to reports of unintended detector motion that may cause patient compression injuries.

    Product
    The Siemens Symbia S series is intended for use by appropriately trained health care professionals to aid in detecting, localizing, diagnosing, staging and restaging of lesions, tumors, disease and organ function for the evaluation of diseases and disorders such as, but not limit
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0912-2015·2015-01-14

    Siemens Symbia T Series SPECT/CT Systems Recalled for Detector Motion

    Siemens Medical Solutions USA is recalling 1,330 Symbia T series SPECT/CT systems worldwide due to reports of unintended radial detector motion that may cause patient compression injuries.

    Product
    The Siemens Symbia T series is intended for use by appropriately trained health care professionals to aid in detecting, localizing, diagnosing, staging and restaging of lesions, tumors, disease and organ function for the evaluation of diseases and disorders such as, but not limit
    Category
    Medical Device
    Distribution
    0 states