BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 1232569 · Received November 13, 2008

    Report

    Report Number
    1720753-2008-27997
    Event Type
    Malfunction
    Date Received
    November 13, 2008
    Date of Event
    October 23, 2008
    Report Date
    November 12, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MS, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THIS MDR IS RELATED TO GE HEALTHCARE COMPLAINT NUMBER. THE GE SERVICE REP VERIFIED THE SYMPTOM, AND REPLACED BOTH WORKSTATION MONITORS. HE CHECKED THE MONITORS AND VERIFIED NICE CLEAR IMAGES. HE VERIFIED PROPER OPERATION OF THE SYSTEM.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE LOCKS ON THE SYSTEM ARE LOOSE AND THE MONITORS ON THE WORKSTATION HAVE A BURN, AND IT IS CAUSING THE DOCTOR PROBLEMS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1