BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FLEXTEND IS-1 BI POSITIVE FIX

    MDR report key: 1043101 · Received May 8, 2008

    Report

    Report Number
    2124215-2008-33546
    Event Type
    Malfunction
    Date Received
    May 8, 2008
    Date of Event
    February 15, 2008
    Report Date
    February 15, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    DTB
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLEXTEND IS-1 BI POSITIVE FIX IMPLANTABLE LEAD DTB CARDIAC PACEMAKERS, INC 4088 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Other THE DEVICE 1290/722359 WAS IMPLANTED 04-AUG-2005| THE DEVICE 4469/447523 WAS IMPLANTED 04-AUG-2005| THE DEVICE 4470/475576 WAS IMPLANTED 04-AUG-2005