BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VITALITY 2 VR

    MDR report key: 1043598 · Received May 8, 2008

    Report

    Report Number
    2124215-2008-33035
    Event Type
    Malfunction
    Date Received
    May 8, 2008
    Date of Event
    January 31, 2008
    Report Date
    January 31, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    LWS
    Removal / Correction Number
    Z47/53-08
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    LAY USER/PATIENT

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VITALITY 2 VR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR LWS CARDIAC PACEMAKERS, INC T175 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 77 YR Other THE DEVICE 6481 029404 WAS USED DURING THE EVENT.| THE DEVICE 0184/101586 WAS IMPLANTED 02-DEC-2004