BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ATLAS II PLUS HF CRT-D

    MDR report key: 4091589 · Received January 13, 2014

    Report

    Report Number
    2938836-2014-04908
    Event Type
    Malfunction
    Date Received
    January 13, 2014
    Date of Event
    December 5, 2011
    Manufacturer
    ST. JUDE MEDICAL INC., CRMD
    Product Code
    NIK
    PMA / PMN Number
    P030054
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ALL INFO PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED. THIS HISTORICAL COMPLAINT IS BEING FILED AS PART OF A RETROSPECTIVE REVIEW OF COMPLAINT FILES IN RESPONSE TO A RECENT FDA INSPECTION. THERE IS NO CHANGE TO THE ACTUAL PERFORMANCE OF THE PRODUCT AND THIS REPORT ONLY REPRESENTS AN ENHANCEMENT TO THE REPORTING CRITERIA GOING FORWARD.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT POST PACED T WAVE OVERSENSING ON THE VENTRICULAR LEAD WAS NOTED. PATIENT DID NOT RECEIVE THERAPY. DECREASE VENTRICULAR SENSITIVITY WAS RECOMMENDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    23186 ATLAS II PLUS HF CRT-D IMPLANTABLE CARDIOVERTER DEFIBRILLATOR, NIK NIK ST. JUDE MEDICAL INC., CRMD V-366

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR