BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 3894394 · Received April 23, 2014

    Report

    Report Number
    1720753-2014-03579
    Event Type
    Malfunction
    Date Received
    April 23, 2014
    Date of Event
    April 10, 2014
    Report Date
    April 23, 2014
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REPRESENTATIVE PERFORMED AN ON SITE INVESTIGATION. THE INTERCONNECT CABLE WAS EVALUATED AND REPLACED. THE VIDEO BOARD WAS RESEATED. THE VOLTAGE ON 5V POWER SUPPLY WAS RE-ADJUSTED. THE SYSTEM WAS TESTED AND FOUND TO BE WORKING AS INTENDED AND RETURNED TO SERVICE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT X-RAYS WERE DISABLED. THIS RESULTED IN A LOSS OF IMAGING FUNCTIONALITY. THERE IS NO REPORT OF INJURY OR DEATH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    247290 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9800

    Patients

    Seq Age Sex Outcome Treatment
    1