BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERITY DR

    MDR report key: 4143002 · Received January 13, 2014

    Report

    Report Number
    2017865-2014-05603
    Event Type
    Malfunction
    Date Received
    January 13, 2014
    Date of Event
    December 15, 2011
    Manufacturer
    ST. JUDE MEDICAL, CRMD
    Product Code
    DXY
    PMA / PMN Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    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. INITIAL REPORTER: TECH SERV SPECIALIST.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PULSE GENERATOR EXHIBITED LOW LEAD IMPEDANCE ON THE ATRIAL CHANNEL. THE DEVICE REMAINS IMPLANTED AND THE PT WILL CONTINUE TO BE MONITORED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    32134 VERITY DR IMPLANTABLE PACEMAKER PULSE GENERATOR DXY ST. JUDE MEDICAL, CRMD 5356

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR