BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ENDOTAK RELIANCE G

    MDR report key: 1042104 · Received May 8, 2008

    Report

    Report Number
    2124215-2008-34535
    Event Type
    Injury
    Date Received
    May 8, 2008
    Date of Event
    March 18, 2008
    Report Date
    March 18, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    LWS
    Removal / Correction Number
    NA
    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 ENDOTAK RELIANCE G IMPLANTABLE LEAD LWS CARDIAC PACEMAKERS, INC 0185 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 75 YR Required Intervention THE DEVICE H217/709982 WAS IMPLANTED 12-SEP-2007| THE DEVICE 6483 507020 WAS USED DURING THE EVENT.| THE DEVICE 4554/159725 WAS IMPLANTED 12-SEP-2007| THE DEVICE 4470/555022 WAS IMPLANTED 12-SEP-2007| THE DEVICE 6487 507030 WAS USED DURING THE EVENT.| THE DEVICE 6482 025737 WAS USED DURING THE EVENT.