BEUDAMED
    FDA Adverse Event Injury Summary report: N

    G.E. MEDICAL SYSTEMS

    MDR report key: 280631 · Received May 23, 2000

    Report

    Report Number
    280631
    Event Type
    Injury
    Date Received
    May 23, 2000
    Date of Event
    May 18, 2000
    Report Date
    May 23, 2000
    Manufacturer
    GE MEDICAL SYSTEMS
    Product Code
    JAA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    IN, US
    Reporter Occupation
    RADIOLOGIC TECHNOLOGIST

    Narratives

    Description of Event or Problem · 1

    DR LEANED ACROSS PT TO LOOK AT SCREEN. THEIR BODY PRESSED AGAINST IMAGE INTENSIFIER CONTROL. IMAGE INTENSIFIER LOWERED ON TO PT, BREAKING THEIR RIB. IMAGE INTENSIFIER SYSTEM SAFETY SWITCH FAILED TO STOP DRIVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 G.E. MEDICAL SYSTEMS ADVNTX AFM SPECIAL PROCEDURES RM JAA GE MEDICAL SYSTEMS 46-276233GI *

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Required Intervention