BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MRI

    MDR report key: 1603994 · Received February 17, 2010

    Report

    Report Number
    MW5014736
    Event Type
    Injury
    Date Received
    February 17, 2010
    Date of Event
    December 2, 2009
    Report Date
    February 17, 2010
    Manufacturer
    G.E.
    Product Code
    LNH
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    VT, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    MRI (B) (6) 2009. DURING MRI, PT EXPERIENCED WARMING IN PELVIS AND LEFT ARM. PROCEDURE HAD TO BE STOPPED DUE TO DISCOMFORT. PT APPLIED ICE PACKS FOR THE REMAINDER OF THE DAY AND EVENING. PT STILL EXPERIENCES PAIN ON AND OFF IN RIGHT HIP. PT IS MAKING FORMAL WRITTEN COMPLAINT AT USER FACILITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MRI MRI LNH G.E.

    Patients

    Seq Age Sex Outcome Treatment
    1 46 YR Other