BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 3182526 · Received June 14, 2013

    Report

    Report Number
    1720753-2013-07118
    Event Type
    Malfunction
    Date Received
    June 14, 2013
    Date of Event
    June 5, 2013
    Report Date
    June 14, 2013
    Manufacturer
    GE OEC MEDICAL SYSTEMS SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REPRESENTATIVE PERFORMED AN ONSITE INVESTIGATION. THE HIGH VOLTAGE CABLE AND X-RAY TUBE WERE REPLACED. THE SYSTEM WAS THEN FOUND TO BE OPERATING AS INTENDED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYSTEM DISPLAYED A STATOR NOT ON ERROR MESSAGE. THIS ERROR MESSAGE WILL LIKELY CAUSE THE SYSTEM TO SHUT DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    272305 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS SLC) 9900

    Patients

    Seq Age Sex Outcome Treatment
    1