BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GE MRI

    MDR report key: 17097508 · Received June 8, 2023

    Report

    Report Number
    MW5118276
    Event Type
    Injury
    Date Received
    June 8, 2023
    Report Date
    May 15, 2023
    Manufacturer
    GE HEALTHCARE MANUFACTURING LLC
    Product Code
    LNH
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    OXYGEN TANK PULLED INTO MRI SCANNER AT (B)(6) HOSPITAL IN (B)(6). PATIENT WAS IN THE SCANNER AT THE TIME AND WAS STRUCK ON THE FEET. PATIENT WAS UNDER ANESTHESIA AT THE TIME. EVENT WAS NEVER REPORTED AND A COMPANY OTHER THAN THE MANUFACTURER WAS SOLICITED TO REMOVE THE TANK. EVENT WAS COVERED UP. REFERENCE REPORT: MW5118277.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2208440 GE MRI SYSTEM, NUCLEAR MAGNETIC RESONANCE IMAGING LNH GE HEALTHCARE MANUFACTURING LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Required Intervention