BEUDAMED
    FDA Adverse Event Other Summary report: N

    7700

    MDR report key: 982335 · Received January 22, 2008

    Report

    Report Number
    9680959-2008-00009
    Event Type
    Other
    Date Received
    January 22, 2008
    Date of Event
    January 10, 2008
    Report Date
    January 22, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE SERVICE REP CHECKED THE MONITOR ROTATION FUNCTIONS, AS WELL AS THE AUTO ROTATION FUNCTIONS, AND FOUND NO PROBLEMS. HE EXAMINED THE INTERIOR FOR ANY OBVIOUS DEFECTS, BUT FOUND NONE. CHECKED ALL CONNECTOR AND WIRING FOR INTEGRITY. CHECKED OVERALL OPERATION AND VERIFIED THE SYSTEM PERFORMS AS INTENDED. THE PROBLEM COULD NOT BE DUPLICATED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE MONITOR CONTINUALLY ROTATES AND DISPLAYS LINES. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 7700 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1