BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PATIENT BED

    MDR report key: 1873918 · Received September 22, 2010

    Report

    Report Number
    1873918
    Event Type
    Malfunction
    Date Received
    September 22, 2010
    Date of Event
    September 21, 2010
    Report Date
    September 22, 2010
    Manufacturer
    HILL-ROM
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NY, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    WHILE PATIENT CARE WAS BEING PERFORMED, PATIENT'S BED DROPPED TO THE LOWEST POSITION. THERE WERE NO REPORTED INJURIES TO PATIENT OR STAFF. THE BED WAS REMOVED FROM SERVICE BY HOUSEKEEPING AND REPLACED WITH NEW BED. A REPAIR COMPANY IS SCHEDULED FOR A VISIT TO REPAIR AND TEST THE BED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PATIENT BED PATIENT BED FNL HILL-ROM VERSA CARE TM *

    Patients

    Seq Age Sex Outcome Treatment
    1 92 YR