BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MEDTRONIC

    MDR report key: 2171284 · Received July 18, 2011

    Report

    Report Number
    MW5021391
    Event Type
    Malfunction
    Date Received
    July 18, 2011
    Product Code
    LGW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    EMF-EMI SENSATIONS/ "ZINGS" AROUND ELECTRONICS IE: COMPUTERS, CELL PHONES, GAS PUMPS, MICROWAVES, GROCERY CHECKOUTS STARTING A VEHICLE LIGHTNING IS AWFUL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDTRONIC SPINAL CORD STIMULATOR LGW 37702

    Patients

    Seq Age Sex Outcome Treatment
    1 46 YR