BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ENERGEN

    MDR report key: 3905689 · Received July 1, 2014

    Report

    Report Number
    2124215-2014-11337
    Event Type
    Injury
    Date Received
    July 1, 2014
    Date of Event
    May 20, 2014
    Report Date
    May 20, 2014
    Manufacturer
    GUIDANT CRM CLONMEL IRELAND
    Product Code
    LWP
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). 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 THE PATIENT IMPLANTED WITH THIS DEVICE SYSTEM WAS PRESENTED AND ADMITTED TO THE EMERGENCY ROOM WITH SYMPTOMS OF CONGESTIVE HEART FAILURE (CHF) AND A REPORTED SYNCOPAL EPISODE. THE DEVICE WAS INTERROGATED AND NO THERAPY HAD BEEN DELIVERED. THE PATIENT'S CARDIOLOGIST MADE NO PROGRAMMING CHANGES TO THE DEVICE. NO FURTHER INFORMATION WAS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    384052 ENERGEN IMPLANTABLE CARDIOVERTER DEFIBRILLATOR LWP GUIDANT CRM CLONMEL IRELAND N141

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR Life Threatening N141| 4470| 4518| 0185