BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RIATA ACTIVE FIXATION

    MDR report key: 1954984 · Received January 10, 2011

    Report

    Report Number
    2017865-2011-00089
    Event Type
    Malfunction
    Date Received
    January 10, 2011
    Date of Event
    September 28, 2010
    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
    DC
    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 HIGH THRESHOLDS WERE NOTED ON THE RV CHANNEL. WHEN THE DEVICE WAS REPLACED AND THE NEW DEVICE WAS CONNECTED TO THE ORIGINAL LEAD, THE THRESHOLDS DECREASED CONSIDERABLY BUT WERE STILL HIGH. THE PHYSICIAN SUSPECTED A PROBLEM WITH THE RV CONNECTOR PART OF THE ICD. THE LEAD REMAINS IMPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RIATA ACTIVE FIXATION DEFIBRILLATION LEAD NVY ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION 1581/60 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR (B)(4)