BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DEXTRUS 4136

    MDR report key: 1004019 · Received February 25, 2008

    Report

    Report Number
    1028232-2008-00146
    Event Type
    Injury
    Date Received
    February 25, 2008
    Date of Event
    December 13, 2007
    Report Date
    January 29, 2008
    Manufacturer
    BIOTRONIK GMBH AND CO.
    Product Code
    DTB
    PMA / PMN Number
    P950037
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    BOSTON SCIENTIFIC CRM RECEIVED INFORMATION THAT THIS DEXTRUS ATRIAL LEAD DISLODGED, AND WAS SUCCESSFULLY REPOSITIONED IN A REVISION PROCEDURE. NO ADVERSE PATIENT EFFECTS WERE REPORTED. BSC WAS UNABLE TO PROVIDE IMPLANT DATES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DEXTRUS 4136 PACER LEAD DTB BIOTRONIK GMBH AND CO. 358754

    Patients

    Seq Age Sex Outcome Treatment
    1 YR Hospitalization