BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    QUADRA ASSURA CRT-D, DF4 CONNECTOR

    MDR report key: 3080171 · Received April 26, 2013

    Report

    Report Number
    2938836-2013-01024
    Event Type
    Malfunction
    Date Received
    April 26, 2013
    Date of Event
    March 4, 2013
    Manufacturer
    ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
    Product Code
    NIK
    PMA / PMN Number
    P910023
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY
    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

    NEW INFORMATION NOTES THAT REPROGRAMMING WAS PERFORMED. ISSUE WAS RESOLVED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT OVERSENSING WAS OBSERVED WHEN PATIENT PRESENTED IN CLINIC AFTER RECEIVING A VIBRATORY ALERT. THE PATIENT DID NOT HAVE ANY SYMPTOM. IT WAS RECOMMENDED TO REPROGRAM THE DEVICE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    182847 QUADRA ASSURA CRT-D, DF4 CONNECTOR IMPLANATABLE CARDIOVERTER DEFIBRILLATOR NIK ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION CD3265-40Q NA

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR