BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2600

    MDR report key: 1021706 · Received March 19, 2008

    Report

    Report Number
    1720753-2008-19688
    Event Type
    Malfunction
    Date Received
    March 19, 2008
    Date of Event
    March 5, 2008
    Report Date
    March 17, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS, INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SVC REP PERFORMED AN ON SITE INVESTIGATION. THE REPORTED FAILURE COULD NOT BE DUPLICATED. THE SYSTEM WAS TESTED AND FOUND TO BE WORKING AS INTENDED AND PLACED BACK INTO SVC.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE 2600 SYSTEM DISPLAYED A "COLLIMATOR HOLD" AND THE SYSTEM WOULD NOT FLUORO. THERE WAS NO REPORT OF PT INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 2600 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS, INC. 2600 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK