BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FINELINE I

    MDR report key: 3240095 · Received July 22, 2013

    Report

    Report Number
    2124215-2013-10279
    Event Type
    Injury
    Date Received
    July 22, 2013
    Date of Event
    May 13, 2013
    Report Date
    May 22, 2013
    Manufacturer
    CPI - DEL CARIBE
    Product Code
    NVN
    PMA / PMN Number
    P960004
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA
    Reporter Occupation
    PHYSICIAN

    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 PRODUCT WAS PART OF A SYSTEM REVISION DUE TO INFECTION. THERE WERE NO ADDITIONAL ADVERSE EFFECTS REPORTED. THE PRODUCT WAS EXPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    339788 FINELINE I IMPLANTABLE LEAD NVN CPI - DEL CARIBE 4461

    Patients

    Seq Age Sex Outcome Treatment
    1 79 YR Hospitalization| L| R 1851| 0155| N119| 4537| 4470| 7271| 4461| H177