BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VITALITY DS VR

    MDR report key: 1043128 · Received May 8, 2008

    Report

    Report Number
    2124215-2008-33517
    Event Type
    Injury
    Date Received
    May 8, 2008
    Date of Event
    February 13, 2008
    Report Date
    March 4, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    LWS
    Removal / Correction Number
    Z47/53-08
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VITALITY DS VR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR LWS CARDIAC PACEMAKERS, INC T135 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Required Intervention THE DEVICE 0125/230198 WAS IMPLANTED 02-OCT-1998| THE DEVICE T175/129988 WAS IMPLANTED 13-FEB-2008