BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TENDRIL DX

    MDR report key: 2905198 · Received January 9, 2013

    Report

    Report Number
    2017865-2013-00506
    Event Type
    Malfunction
    Date Received
    January 9, 2013
    Date of Event
    November 19, 2012
    Manufacturer
    ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
    Product Code
    NVN
    PMA / PMN Number
    P960013
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    RELIABILITY LABORATORY TECHNICIAN, NOT APPLICABLE. - ST. JUDE MEDICAL (B)(4) RELIABILITY LABORATORY. NO COMPLAINT WAS RECEIVED WITH RETURN OF THE DEVICE. FAILURE (EVENT) OBSERVED DURING ANALYSIS. FINAL ANALYSIS FOUND THAT THE LEAD WAS RETURNED IN TWO PIECES. THE OUTER INSULATION WAS ABRADED AT 13.0 CM TO 13.3 CM FROM THE PIN AND EXPOSED THE OUTER COIL. ABRASIONS ARE INDICATIVE OF CONSTANT FRICTION WITH ANOTHER IMPLANTABLE DEVICE.

    Description of Event or Problem · 1

    THIS REPORT IS TO ADVISE OF AN EVENT OBSERVED DURING ANALYSIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    11933 TENDRIL DX PERMANENT PACEMAKER ELECTRODE NVN ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION 1388T/46 NA

    Patients

    Seq Age Sex Outcome Treatment
    1