The Recall Desk

Hazard

Quality System Non Compliance recalls

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

What the numbers show

Total
178
Critical
0
Severe
0
Most recent
2023-11-01

Of the 178 quality system non compliance 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 quality system non compliance 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.

176–178 of 178

  • ModerateFDA (Devices)·Z-1913-2014·2014-07-02

    Anspach Custom Devices Recalled for Quality System Non-Compliance

    The Anspach Effort, Inc. is recalling Anspach Custom Devices because they were not manufactured consistently with Quality System requirements.

    Product
    ANSPACH***REF SP-4604-00***3mm Fluted Ball for Adjustable 25cm Mia Attachment***Rx Only*** This device is intended to be used with Anspach Systems
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1906-2014·2014-07-02

    Anspach Recalls 113 MRI Fluted Routers for Quality System Non-Compliance

    The Anspach Effort, Inc. is recalling 113 MRI fluted routers because they were not manufactured consistently with Quality System requirements.

    Product
    ANSPACH***1.85mm x 16 mm Fluted Router for MRI***Rx Only*** This device is intended to be used with Anspach Systems
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1918-2014·2014-07-02

    Anspach Custom Shoulder Implant Recalled for Quality System Non-Compliance

    The Anspach Effort, Inc. is recalling custom shoulder implants because they were not manufactured consistently with Quality System requirements.

    Product
    ANSPACH***REF 98-0012***Shoulder Implant 011mm Rod, 20cm Long, Custom***Rx Only*** This device is intended to be used with Anspach Systems
    Category
    Medical Device
    Distribution
    14 states