BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIGHTSPEED LS QXI

    MDR report key: 732138 · Received July 6, 2006

    Report

    Report Number
    2126677-2006-00013
    Event Type
    Other
    Date Received
    July 6, 2006
    Date of Event
    June 4, 2006
    Report Date
    July 6, 2006
    Manufacturer
    GE MEDICAL SYSTEMS, LLC
    Product Code
    JAK
    Report Source
    Manufacturer report
    Reporter Location
    NY
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE NURSING STAFF STATED THAT THEY TRIED TO PRESS THE GANTRY E-STOP BUTTONS, BUT TABLE MOTION DID NOT HALT. A GE SERVICE REP PERFORMED AN ON SITE EVAL. THE SYSTEM AND E-STOP WERE FOUND TO BE OPERATING TO SPEC. PROBLEMS WITH THE E-STOP COULD NOT BE DUPLICATED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT NURSING STAFF WERE IN THE CT ROOM DURING A PT CODE. NO TRAINED CT PERSONNEL WERE IN THE ROOM AT THAT TIME. A NURSE INADVERTENTLY STEPPED ON THE CT TABLE UP FOOT PEDAL CAUSING ANOTHER NURSE, STANDING BY THE GENTRY END OF THE TABLE, TO BE PUSHED UP AND THROUGH THE CT GENTRY BORE. INJURIES THAT INCLUDED ABRASIONS AND CONTUSIONS TO THE TORSO AREA ALONG WITH UPPER LUMBAR ACHING. NO OTHER SERIOUS INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIGHTSPEED LS QXI CT JAK GE MEDICAL SYSTEMS, LLC 2180482 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR