BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 2100251 · Received May 16, 2011

    Report

    Report Number
    1720753-2011-07365
    Event Type
    Malfunction
    Date Received
    May 16, 2011
    Date of Event
    May 9, 2011
    Report Date
    May 16, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    EI
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REPRESENTATIVE PERFORMED AN ONSITE INVESTIGATION. THE INTERCONNECT CABLE AND THE POWER CONTROL PRINTED CIRCUIT BOARD WERE REPLACED AND THE LOOSE C-ARM CONNECTOR PINS WERE REFITTED. THE SYSTEM WAS TESTED AND FOUND TO BE WORKING AS INTENDED AND PUT BACK INTO SERVICE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYSTEM PRODUCED A FLASH EXPOSURE BUT WOULD NOT DISPLAY IMAGES WHEN THEY WERE SCANNED AND THER WAS NO POWER TO THE C-ARM. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9800

    Patients

    Seq Age Sex Outcome Treatment
    1