BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TVL LEAD, RIGHT VENTRICULAR

    MDR report key: 2984516 · Received February 28, 2013

    Report

    Report Number
    2938836-2013-00585
    Event Type
    Malfunction
    Date Received
    February 28, 2013
    Date of Event
    January 14, 2013
    Manufacturer
    ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
    Product Code
    NVY
    PMA / PMN Number
    P950022
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AR
    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 THE LEAD WAS CAPPED AND REPLACED DUE TO AN INSULATION ANOMALY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    89028 TVL LEAD, RIGHT VENTRICULAR DEFIBRILLATION LEAD NVY ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION RV02 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR