BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GE HEALTHCARE

    MDR report key: 1445413 · Received August 19, 2009

    Report

    Report Number
    MW5012499
    Event Type
    Injury
    Date Received
    August 19, 2009
    Date of Event
    August 11, 2009
    Report Date
    August 19, 2009
    Manufacturer
    GE HEALTHCARE
    Product Code
    LNH
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MT, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    PT WAS HAVING AN MRI OF HIS SHOULDER. PT COMPLAINED OF A BURNING SENSATION ON HIS RIGHT THUMB AND RIGHT THIGH WHICH WERE IN CONTACT WITH EACH OTHER. WHEN PT WAS REMOVED FROM MRI MACHINE, MRI TECH OBSERVED A 1/2" BLISTER ON HIS RIGHT THUMB AND RIGHT THIGH. DOCTOR WAS NOTIFIED. PT WAS TREATED FOR BURN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GE HEALTHCARE * LNH GE HEALTHCARE 3T HD 8CH-400-AP *

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Disability