BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FINELINE II

    MDR report key: 1042891 · Received May 8, 2008

    Report

    Report Number
    2124215-2008-33754
    Event Type
    Injury
    Date Received
    May 8, 2008
    Date of Event
    February 20, 2008
    Report Date
    February 20, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    DTB
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FINELINE II IMPLANTABLE LEAD DTB CARDIAC PACEMAKERS, INC 4471 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 37 YR Required Intervention THE DEVICE 1280/546036 WAS IMPLANTED 02-JAN-2003| THE DEVICE 1291/147186 WAS IMPLANTED 20-FEB-2008| THE DEVICE 4470/352971 WAS IMPLANTED 14-APR-2003| THE DEVICE 4471/454744 WAS IMPLANTED 20-FEB-2008