BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 1173038 · Received September 19, 2008

    Report

    Report Number
    1720753-2008-26048
    Event Type
    Malfunction
    Date Received
    September 19, 2008
    Date of Event
    September 5, 2008
    Report Date
    September 18, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE GE SERVICE REP SPOKE WITH THE CUSTOMER AND CONFIRMED THE PROBLEM REPORTED. HE CHECKED THE SYSTEM AND FOUND THE INTERCONNECT CABLE WAS DAMAGED CAUSING THE WORKSTATION TO LOOSE CONNECTION WITH THE GENERATOR. THE REP REMOVED AND REPLACED THE INTERCONNECT CABLE, THE FLASHED NODES, AND REBUILT THE SYSTEM FILES. THE MACHINE WORKS AS INTENDED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE SYSTEM INTERMITTENTLY FLUOROS. THE CUSTOMER MUST REBOOT THE SYSTEM TO CONTINUE WITH THE FLUORO.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1