BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IDENTITY ADX DR

    MDR report key: 4143039 · Received January 13, 2014

    Report

    Report Number
    2017865-2014-05611
    Event Type
    Malfunction
    Date Received
    January 13, 2014
    Date of Event
    December 21, 2011
    Manufacturer
    ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISION
    Product Code
    DXY
    PMA / PMN Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    ALL INFO PROVIDED BY MFR, 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 THE PT PRESENTED IN CLINIC FOR SCHEDULED CHECK. THE PULSE GENERATOR EXHIBITED INAPPROPRIATE MEASURED DATA. THE DEVICE WAS SCHEDULED FOR CHANGEOUT DEU TO ERI.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    31722 IDENTITY ADX DR IMPLANTABLE PACEMAKER PULSE GENERATOR DXY ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISION 5380

    Patients

    Seq Age Sex Outcome Treatment
    1 79 YR