The Recall Desk

Hazard

Non Compliance recalls

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

What the numbers show

Total
85
Critical
0
Severe
4
Most recent
2026-09-10

Of the 85 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 4 (5%) 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 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.

76–85 of 85

  • ModerateFDA (Devices)·Z-0265-2013·2012-11-14

    Shimadzu Recalls Mobile X-ray Systems for Beam Quality Non-Compliance

    Shimadzu Medical Systems is recalling 3 mobile X-ray systems because they may not meet federal beam quality standards.

    Product
    0.4/0.7JG326D-265AX/AT Product Usage: The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannot move and/or of outpatients in emergency.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0261-2013·2012-11-14

    Shimadzu Recalls Diagnostic X-Ray Beam-Limiting Devices for Performance Non-Compliance

    Shimadzu is recalling 308 R-20J Diagnostic X-Ray Beam-Limiting Devices because they may not meet 2006 FDA performance standards for beam quality.

    Product
    R-20J , Diagnostic X-Ray Beam-Limiting Device. In combination with any of below X-Ray tubes: 06/1.2P364DK-85, 0.6/1.2P324DK-125, 06/1.2P324DK-85, 0.6/1.2P38DE-85. Product Usage: The device is the beam-limiting device for X-ray Radiography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·12V482000·2012-09-03

    Morgan Olson Recalls 2009-2011 Walk-In Vans for Safety Standard Failures

    Morgan Olson is recalling 24 model year 2009-2011 Walk-In Vans because they fail to meet various Federal Motor Vehicle Safety Standards, potentially increasing crash risk.

    Product
    MORGAN OLSON — MORGAN OLSON WALK IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·10V405000·2010-09-09

    Auto Moto Recalls 2009-2010 Scooters for Rear Brake Control Defect

    Zhejiang Xingyue Vehicle Co. is recalling 305 Auto Moto XY150ZK scooters because the rear brake is foot-operated instead of hand-operated, violating federal safety standards.

    Product
    THE AUTO MOTO — THE AUTO MOTO XY150ZK
    Category
    Vehicle
    Distribution
    Distributed nationwide