BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 4090047 · Received August 18, 2014

    Report

    Report Number
    1720753-2014-07050
    Event Type
    Malfunction
    Date Received
    August 18, 2014
    Date of Event
    July 28, 2014
    Report Date
    August 18, 2014
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REP PERFORMED AN ONSITE INVESTIGATION. THE REPORTED ISSUE COULD NOT BE DUPLICATED. THE HIGH VOLTAGE CABLE WAS REPLACED DURING THE SERVICE CALL. 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 WOULD NOT DISPLAY A LIVE IMAGE AND WOULD TRACK TO MAXIMUM TECHNIQUE WHEN THE C WAS ROTATED FOR A LATERAL VIEW. THIS MADE THE SYSTEM TEMPORARILY UNUSABLE. THERE IS NO REPORT OF INJURY OR DEATH ASSOCIATED WITH THE EVENT DESCRIBED IN THIS COMPLAINT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    496253 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9900

    Patients

    Seq Age Sex Outcome Treatment
    1