BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FINELINE II

    MDR report key: 2161288 · Received July 13, 2011

    Report

    Report Number
    2124215-2011-07526
    Event Type
    Injury
    Date Received
    July 13, 2011
    Date of Event
    February 17, 2011
    Report Date
    April 14, 2011
    Manufacturer
    CPI - DEL CARIBE
    Product Code
    NVN
    PMA / PMN Number
    P960004
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    AS NO FURTHER INFORMATION CONCERNING THIS REPORT IS EXPECTED, OUR INVESTIGATION IS COMPLETE. THIS INVESTIGATION WILL BE UPDATED SHOULD FURTHER INFORMATION BE PROVIDED.

    Description of Event or Problem · 1

    BOSTON SCIENTIFIC RECEIVED INFORMATION THAT THIS LEAD WAS PART OF A SYSTEM EXPLANT DUE TO A PATIENT INFECTION. THE DEVICE WAS REMOVED AT A LATER DATE. A FRACTURE WAS NOTED ON ONE OF THE LEADS CAUSING BLOOD CLOTS TO FORM, HOWEVER THE SPECIFIC LEAD COULD NOT BE DETERMINED. 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 FINELINE II IMPLANTABLE LEAD NVN CPI - DEL CARIBE 4469

    Patients

    Seq Age Sex Outcome Treatment
    1 32 YR Hospitalization| L| R 5568| 4470| 4469| 1882TC| 1280| S606| 5592