BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2124215-2011-05924

    MDR report key: 2060093 · Received April 15, 2011

    Report

    Report Number
    2124215-2011-05924
    Event Type
    Injury
    Date Received
    April 15, 2011
    Date of Event
    March 31, 2011
    Report Date
    March 31, 2011
    Manufacturer
    GUIDANT PUERTO RICO BV
    Product Code
    LWS
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Additional Manufacturer Narrative · 1

    THE SYSTEM REMAINS IMPLANTED AND NO OTHER ADVERSE EVENTS HAVE BEEN REPORTED. THIS ISSUE WILL BE RE-EVALUATED IF ADDITIONAL INFORMATION IS RECEIVED.

    Description of Event or Problem · 1

    BOSTON SCIENTIFIC RECEIVED INFORMATION THAT A SUBCUTANEOUS EROSION OF THIS POCKET WAS OBSERVED. THE REVISION PROCEDURE WAS PERFORMED AND THE POCKET WAS DRAINED AND CULTURED. NO ADVERSE PATIENT EFFECTS WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LWS GUIDANT PUERTO RICO BV

    Patients

    Seq Age Sex Outcome Treatment
    1 77 YR H217| 0158| 1296| 4017| 4046| 4018| N119| 4543