BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 1813138 · Received August 18, 2010

    Report

    Report Number
    1824206-2010-09401
    Event Type
    Malfunction
    Date Received
    August 18, 2010
    Date of Event
    July 23, 2010
    Report Date
    July 23, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE NURSE LOCKOUT HEAD DOWN WAS NOT WORKING. THE TECHNICIAN REPLACED THE NURSE LOCKOUT BOX TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE BED HAS NO HEAD DOWN FUNCTIONS. NO ALLEGED INJURIES BY THE ACCOUNT. THE HEAD OF THE BED IS ABLE TO GO UP AFTER CHANGING THE CONTROL BOX BUT WILL NOT GO DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESIDENT BED AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 870

    Patients

    Seq Age Sex Outcome Treatment
    1