BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CARELINK

    MDR report key: 4160976 · Received October 10, 2014

    Report

    Report Number
    2182208-2014-02769
    Event Type
    Malfunction
    Date Received
    October 10, 2014
    Date of Event
    July 8, 2014
    Report Date
    July 8, 2014
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    KRG
    PMA / PMN Number
    P890003
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS EVENT OCCURRED OUTSIDE THE US WHERE THE SAME MODEL IS DISTRIBUTED. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS. (B)(4)

    Description of Event or Problem · 1

    IT WAS REPORTED THAT AN ERROR MESSAGE DISPLAYED DURING A DEVICE INTERROGATION. THE PROGRAMMER WAS CYCLE POWERED, BUT THE SAME ERROR CODE DISPLAYED ON DEVICE INTERROGATION. SUCCESSFUL DEVICE INTERROGATION WAS COMPLETED USING A DIFFERENT PROGRAMMER. THE SALES REPRESENTATIVE RAN THE SERVICE DISK AND THE PROGRAMMER HAS SINCE RETURNED TO NORMAL FUNCTION. THE PROGRAMMER REMAINS IN USE. THERE WAS NO PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    642335 CARELINK PROGRAMMER, PACEMAKER KRG MEDTRONIC, INC. 2090

    Patients

    Seq Age Sex Outcome Treatment
    1