BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VITALITY DS

    MDR report key: 1042990 · Received May 8, 2008

    Report

    Report Number
    2124215-2008-33659
    Event Type
    Malfunction
    Date Received
    May 8, 2008
    Date of Event
    February 19, 2008
    Report Date
    February 19, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    LWS
    Removal / Correction Number
    Z47/53-08
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    LAY USER/PATIENT

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VITALITY DS IMPLANTABLE CARDIOVERTER DEFIBRILLATOR LWS CARDIAC PACEMAKERS, INC T125 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Other THE DEVICE 6481 036765 WAS USED DURING THE EVENT.| THE DEVICE 4086/212424 WAS IMPLANTED 14-OCT-2004| THE DEVICE 0157/124679 WAS IMPLANTED 14-OCT-2004