BEUDAMED
    FDA Adverse Event Other Summary report: N

    COMPAC 40E

    MDR report key: 608205 · Received May 23, 2005

    Report

    Report Number
    9611343-2005-00017
    Event Type
    Other
    Date Received
    May 23, 2005
    Date of Event
    April 27, 2005
    Report Date
    May 23, 2005
    Manufacturer
    GE MEDICAL SYSTEMS S.C.S.
    Product Code
    KPR
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    HOSPITAL SERVICE TECHNICIAN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE HEATHCARE PROFESSIONAL (HCP) WAS MOVING THE PT FROM A ER STRETCHER TO THE X-RAY TABLE WHEN THE COMPEX 40E TABLE TOP MOVED FREELY CAUSING THE PT TO SLIDE ONTO THE FLOOR FROM THE STRETCHER. THE DOCTOR CHECKED THE PT AND NO INJURIES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COMPAC 40E DIAGNOSTIC X-RAY KPR GE MEDICAL SYSTEMS S.C.S. 2225864 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 100 YR