BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CURRENT PLUS DR

    MDR report key: 3210691 · Received July 8, 2013

    Report

    Report Number
    2938836-2013-03370
    Event Type
    Injury
    Date Received
    July 8, 2013
    Date of Event
    May 3, 2013
    Manufacturer
    ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
    Product Code
    LWS
    PMA / PMN Number
    P910023
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NH
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT AN ASYMPTOMATIC PATIENT PRESENTED IN THE ER AFTER RECEIVING INAPPROPRIATE ATP AND HV THERAPY. STORED EGMS SHOWED ATRIAL FIBRILLATION WITH A RAPID VENTRICULAR RESPONSE. THE DEVICE WAS REPROGRAMMED AND PATIENT WILL BE MONITORED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    310398 CURRENT PLUS DR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR LWS ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION CD2211-36 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 60 YR Required Intervention