The Recall Desk

Hazard

Restricted Maneuverability recalls

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

What the numbers show

Total
1
Critical
0
Severe
0
Most recent
2014-04-09

Of the 1 restricted maneuverability 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 restricted maneuverability 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.

1–1 of 1

  • HighFDA (Devices)·Z-1309-2014·2014-04-09

    Siemens Artis Zee Angiographic Systems Recalled for Cable Connection Defect

    Siemens Medical Solutions is recalling nine Artis Zee Angiographic x-ray systems due to an inappropriate cable connection that may cause system failure and restricted gantry maneuverability.

    Product
    Artis Zee Angiographic x-ray systems.
    Category
    Medical Device
    Distribution
    9 states