The Recall Desk

Hazard

Mr Safety 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
0
Severe
0
Most recent
2019-09-04

Of the 5 mr safety 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 mr safety 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

  • ModerateFDA (Devices)·Z-2407-2019·2019-09-04

    Ad-Tech Medical Recalls Depth Electrodes Due to Incorrect MR Safety Labeling

    Ad-Tech Medical Instrument Corporation is recalling depth electrodes because supplemental information incorrectly stated they were approved for use in the MR environment.

    Product
    Depth Electrodes, Foramen Ovale Depth Electrodes, Macro Micro Depth Electrodes, Spencer Probe Depth Electrodes, Wyler Sphenoidal Depth Electrodes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2406-2019·2019-09-04

    Ad-Tech Medical Recalls Subdural Electrodes Due to Incorrect MR Safety Labeling

    Ad-Tech Medical Instrument Corporation is recalling subdural electrodes because supplemental information incorrectly stated they were approved for use in MRI environments.

    Product
    Dual-Sided Interhemispheric, Grid, Intraoperative, Strip, Wyler Subdural Electrodes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2138-2016·2016-07-13

    Synthes Ti Button Plate Recalled for Inaccurate MR Safety Labeling

    Synthes (USA) Products LLC is recalling 6,255 Ti Button Plate units because their MR safety information does not meet current ASTM standards.

    Product
    Synthes Ti Button Plate 7 Holes, Fastener, Fixation, nondegradable, Soft Tissue
    Category
    Medical Device
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-1009-2015·2015-02-04

    Synthes Mandible External Fixator Recalled for Incorrect MR Safe Labeling

    Synthes, Inc. is recalling Mandible External Fixators because updated testing protocols mean the devices can no longer be designated MR Safe, despite previous labeling.

    Product
    The Synthes Mandible External Fixator; all lots of part nos.: 04.305.003 04.305.004 04.305.005 04.305.010 04.305.011 04.305.012 03.305.006 04.305.100 04.305.101 04.305.102 04.305.103 04.305.128 04.305.130 04.305.134 04.305.138 04.305.140 04.305.142 03.305.105
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0117-2014·2013-11-06

    Integra Camino Intracranial Pressure Monitoring Catheters Recalled for Missing MR Safety Labeling

    Integra Limited is recalling specific Camino Intracranial Pressure Monitoring Catheters and Kits because they lack required labeling indicating they are unsafe in MRI environments.

    Product
    Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring Catheters. Product / Catalogue No.s: 110-4B, 110-4BC, 110-4G, 110-4H, 110-4HC, 110-4L, 110-4LC. The fully packaged 110-4B, 110-4H, and 110-4L catheters are also provided as a component in kits that cont
    Category
    Medical Device
    Distribution
    Distributed nationwide