BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PHILIPS MEDICAL SYSTEMS

    MDR report key: 1055492 · Received May 30, 2008

    Report

    Report Number
    MW5007096
    Event Type
    Injury
    Date Received
    May 30, 2008
    Date of Event
    April 22, 2008
    Report Date
    May 30, 2008
    Product Code
    MOS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    DURING THE PROCESS OF AN MRI, PATIENT WAS POSITIONED HEAD FIRST WITH CABLES ON PT'S RIGHT. PADS WERE USED TO SEPARATE THE CABLES AND KEEP THEM AWAY FROM THE PT. THE BURN WAS PROXIMAL ANTERIOR FEMUR AT THE CIRCULAR AREAS WITH THE CABLES ENTER THE COIL. THE DEVICE USED WAS A RF. COIL MODEL TORSO XL 4535.671.41882, 000263. PATIENT HAD ON SCRUBS, LEGS WERE NOT CROSSED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PHILIPS MEDICAL SYSTEMS RF COIL MOS TORSO XL

    Patients

    Seq Age Sex Outcome Treatment
    1 45 YR Disability RF COIL