BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    6800

    MDR report key: 2102753 · Received May 23, 2011

    Report

    Report Number
    1720753-2011-07553
    Event Type
    Malfunction
    Date Received
    May 23, 2011
    Date of Event
    May 12, 2011
    Report Date
    May 23, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REP PERFORMED AN ONSITE INVESTIGATION. THE C-ARM CABLE WAS REPLACED. NO FURTHER REPAIR INFO IS AVAILABLE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYSTEM'S IMAGES WOULD FLASH AND THEN DISPLAY A BLANK WHITE CIRCLE. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 6800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 6800

    Patients

    Seq Age Sex Outcome Treatment
    1