BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INTERVENE

    MDR report key: 1944532 · Received January 3, 2011

    Report

    Report Number
    2124215-2010-19822
    Event Type
    Injury
    Date Received
    January 3, 2011
    Date of Event
    December 1, 2006
    Report Date
    October 6, 2010
    Manufacturer
    GUIDANT ANGLETON/ST. PAUL
    Product Code
    NVY
    PMA / PMN Number
    P940008
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    DUE TO THE NATURE OF THE ISSUE, NO ANALYSIS WILL BE CONDUCTED IF THE PRODUCT IS RETURNED. THIS REPORT WILL BE UPDATED IF ADDITIONAL INFORMATION IS RECEIVED.

    Description of Event or Problem · 1

    BOSTON SCIENTIFIC CRM RECEIVED INFORMATION THAT THIS PRODUCT WAS PART OF A SYSTEM EXPLANT DUE TO A PATIENT INFECTION. THERE WAS NO REPORT OF ADVERSE PATIENT EFFECTS DUE TO THE EXPLANT PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INTERVENE IMPLANTABLE LEAD NVY GUIDANT ANGLETON/ST. PAUL 497-23

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR Required Intervention 497-23| 101-10