BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ECT

    MDR report key: 1574859 · Received January 6, 2010

    Report

    Report Number
    MW5014255
    Event Type
    Injury
    Date Received
    January 6, 2010
    Date of Event
    January 10, 2000
    Report Date
    January 6, 2010
    Product Code
    GXC
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    ADVERSE EVENT ASSOCIATED WITH THE USE OF AN ECT DEVICE THAT HAS CAUSED EXTENSIVE PROBLEMS AND ON GOING MEMORY LOSS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ECT GXC

    Patients

    Seq Age Sex Outcome Treatment
    1 45 YR