BEUDAMED
    FDA Adverse Event Injury Summary report: N

    QED KNEE COIL

    MDR report key: 3453182 · Received October 31, 2013

    Report

    Report Number
    MW5032527
    Event Type
    Injury
    Date Received
    October 31, 2013
    Date of Event
    October 29, 2013
    Report Date
    October 30, 2013
    Manufacturer
    QED
    Product Code
    MOS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PT HAVING A MRI EXAM OF RIGHT KNEE. ALMOST AT END OF THE EXAM PT COMPLAINT OF KNEE BURNING. EXAM STOPPED RN AND RADIOLOGIST EXAMINED PT. SMALL ARE OF PINKISH / RED AREA ON ANTERIOR RIGHT KNEE, WHICH APPEARED TO BE A (POSSIBLE) BURN FROM THE COIL. PT STATED THAT HIS SYMPTOMS WERE PRETTY MUCH GONE. PT ADVISED THAT IF SYMPTOMS SEEM TO GET WORSE TO CONTACT HIS PHYSICIAN OR TO GO TO THE LOCAL EMERGENCY ROOM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    560239 QED KNEE COIL QED KNEE COIL MOS QED

    Patients

    Seq Age Sex Outcome Treatment
    1 15 YR Other