BEUDAMED
    FDA Adverse Event Injury Summary report: N

    STERIS OPERATING ROOM TABLE

    MDR report key: 6178214 · Received December 13, 2016

    Report

    Report Number
    6178214
    Event Type
    Injury
    Date Received
    December 13, 2016
    Date of Event
    December 6, 2016
    Report Date
    December 9, 2016
    Manufacturer
    STERIS
    Product Code
    FQO
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NC, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    AT END OF PROCEDURE, IT WAS REQUESTED THAT THE BED POSITION BE CHANGED. CRNA UTILIZED CONTROL BUTTON TO CHANGE POSITION, BED CONTINUED TO MOVE IN A FLEX POSITION AFTER SHE LET GO OF CONTROLS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    819831 STERIS OPERATING ROOM TABLE STERIS OPERATING ROOM TABLE FQO STERIS 3085P PRODUCT #

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Required Intervention