BEUDAMED
    FDA Adverse Event Injury Summary report: N

    QUARTET

    MDR report key: 4231327 · Received November 6, 2014

    Report

    Report Number
    2017865-2014-18124
    Event Type
    Injury
    Date Received
    November 6, 2014
    Date of Event
    September 18, 2014
    Manufacturer
    ST. JUDE MEDICAL, INC., CRMD
    Product Code
    OJX
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED. EVALUATION DESCRIPTION INCLUDED. FINAL ANALYSIS FOUND NORMAL DEVICE CHARACTERISTICS.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT PATIENT EXPERIENCED PHRENIC NERVE STIMULATION WITH LEFT VENTRICULAR LEAD. THE LEAD WAS EXPLANTED AND NEW LEAD PLACED IN A NEW TARGET VEIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    714909 QUARTET PERMANENT PACEMAKER ELECTRODE OJX ST. JUDE MEDICAL, INC., CRMD 1458Q/75 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention