BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CARELINK

    MDR report key: 4161038 · Received October 10, 2014

    Report

    Report Number
    2182208-2014-02748
    Event Type
    Malfunction
    Date Received
    October 10, 2014
    Date of Event
    July 24, 2014
    Report Date
    July 24, 2014
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    KRG
    PMA / PMN Number
    P890003
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. PRODUCT EVENT SUMMARY: ANALYSIS COULD NOT CONFIRM THAT THE PROGRAMMER WOULD NOT BOOT UP, HOWEVER, THE PROGRAMMER DOES HAVE A LONG BOOT. AS A RESULT THE HARD DRIVE WAS RECONFIGURED AND SOFTWARE WAS REINSTALLED. IT WAS ALSO NOTED THAT THE STYLUS WAS BENT BUT STILL FUNCTIONAL, THE KEYBOARD SLIDE COVER WAS MISSING, THE KEYBOARD WAS PULLING APART, THE SYSTEM FAN WAS NOISY AND THE LEFT KEYBOARD HINGE WAS BROKEN. (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PROGRAMMER WOULD NOT BOOT UP. THE PROGRAMMER HAS BEEN RETURNED FOR REPAIR. THERE WAS NO PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    642527 CARELINK PROGRAMMER, PACEMAKER KRG MEDTRONIC, INC. 2090

    Patients

    Seq Age Sex Outcome Treatment
    1 2067 RADIOFREQUENCY (RF) HEAD