BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ANTHEM CRT

    MDR report key: 4212831 · Received January 13, 2014

    Report

    Report Number
    2017865-2014-05052
    Event Type
    Malfunction
    Date Received
    January 13, 2014
    Date of Event
    November 19, 2012
    Manufacturer
    ST. JUDE MEDICAL, INC. CRMD
    Product Code
    DXY
    PMA / PMN Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    ALL INFORMATION 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. EVALUATION DESCRIPTION: ANALYSIS WAS NORMAL. NO ANOMALY WAS FOUND.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT DURING IMPLANT THE CAPTURE THRESHOLDS OF THE LEADS WERE ELEVATED WHEN CONNECTED TO THE PULSE GENERATOR. LEAD MEASUREMENTS THROUGH THE PSA WERE NORMAL. THE PULSE GENERATOR WAS NOT IMPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    29496 ANTHEM CRT IMPLANTABLE PACEMAKER PULSE GENERATOR DXY ST. JUDE MEDICAL, INC. CRMD PM3112

    Patients

    Seq Age Sex Outcome Treatment
    1