BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SYSTEM, NUCLEAR MAGNETIC RESONANCE IMAGING

    MDR report key: 11313541 · Received February 10, 2021

    Report

    Report Number
    MW5099346
    Event Type
    Injury
    Date Received
    February 10, 2021
    Date of Event
    January 28, 2021
    Report Date
    February 8, 2021
    Manufacturer
    GE HEALTHCARE MANUFACTURING LLC
    Product Code
    LNH
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AK, US
    Reporter Occupation
    501

    Narratives

    Description of Event or Problem · 1

    MRI EVENT- GLIDESCOPE BROUGHT INTO ZONE 4. NO INJURIES. GE ABLE TO REMOVE GLIDESCOPE NO PROBLEM. NO DAMAGE TO EQUIPMENT. DURING AN INTUBATION IN ZONE 4, A CNA BROUGHT IN A GLIDESCOPE, AND IT WAS SUCKED INTO THE MAGNET. NO INJURIES, AND WE WERE ABLE TO PULL THE ITEM OUT OF THE MAGNET. THERE WERE NO ISSUES WITH THE MAGNET OR IMAGE QUALITY ONCE QC WAS PERFORMED AFTER THE INCIDENT. MRI SUPERVISOR OUT ON VACATION, SO THAT'S WHY DELAYED NOTIFICATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    208359 SYSTEM, NUCLEAR MAGNETIC RESONANCE IMAGING LNH GE HEALTHCARE MANUFACTURING LLC

    Patients

    Seq Age Sex Outcome Treatment
    1