BEUDAMED
    FDA Adverse Event Other Summary report: N

    MG GAMMA CAMERA

    MDR report key: 1962616 · Received January 12, 2011

    Report

    Report Number
    MW5018997
    Event Type
    Other
    Date Received
    January 12, 2011
    Date of Event
    January 11, 2011
    Report Date
    January 12, 2011
    Manufacturer
    GE MEDICAL SYSTEMS
    Product Code
    IYX
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    NUCLEAR MEDICINE TECHNICIAN ATTEMPTED TO POSITION THE PT FOR A BONE SCAN. THE BONE SCAN EQUIPMENT MALFUNCTIONED, AND THE TEST COULD NOT START. THE PT'S TEST WAS CANCELLED. THE PT WAS RESCHEDULED TO RETURN ON AN ALTERNATE DAY FOR THE TEST. EQUIPMENT TECHNICIAN WAS NOTIFIED. THERE WAS NO INJURY TO THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MG GAMMA CAMERA IYX GE MEDICAL SYSTEMS SWM4-PAT

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR