BEUDAMED
    FDA Adverse Event Summary report: N

    OR BED

    MDR report key: 33339 · Received June 7, 1996

    Report

    Report Number
    MW1009250
    Date Received
    June 7, 1996
    Date of Event
    May 20, 1996
    Report Date
    May 22, 1996
    Manufacturer
    AMERICAN STERILIZER CO.
    Product Code
    FQO
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    KY, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    HAD PT POSITIONED ON OR BED. FOOT OF BED RAISED, NO ONE KNEW THE CONTROLS. THERE WAS NO APPARENT INJURY BUT BED HAD TO BE UNPLUGGED BEFORE ACTION WOULD STOP. REPAIRMAN CAME IN AND WORKED ON BED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OR BED OPERATING ROOM TABLE FQO AMERICAN STERILIZER CO.

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO