BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DISCOVERY II

    MDR report key: 2042260 · Received April 6, 2011

    Report

    Report Number
    2124215-2011-03158
    Event Type
    Injury
    Date Received
    April 6, 2011
    Date of Event
    January 17, 2011
    Report Date
    January 17, 2011
    Manufacturer
    GUIDANT CLONMEL IRELAND
    Product Code
    NVZ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    A BOSTON SCIENTIFIC TECHNICAL SERVICES CONSULTANT DISCUSSED THE CLINICAL OBSERVATIONS WITH THE CALLER. 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 THIS PACEMAKER IS PROGRAMMED TO AAI AND THE CALLER WAS QUESTIONING LOSS OF ATRIAL CAPTURE. IT WAS NOTED THAT THIS PATIENT IS IN ATRIAL FIBRILLATION INCONSISTENTLY. NO ADVERSE PATIENT EFFECTS WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DISCOVERY II IMPLANTABLE PULSE GENERATOR NVZ GUIDANT CLONMEL IRELAND 1284

    Patients

    Seq Age Sex Outcome Treatment
    1 76 YR 4457| 1284| 4480