BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 2091093 · Received May 12, 2011

    Report

    Report Number
    1824206-2011-02670
    Event Type
    Malfunction
    Date Received
    May 12, 2011
    Date of Event
    April 19, 2011
    Report Date
    April 19, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE BED HAD NO FUNCTIONS. HE ISOLATED THE ISSUE TO THE CONTROL BOX AND REPLACED THE CONTROL BOX TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT STATED THAT THE BED HAS NO FUNCTION, AND THE HEAD SECTION IS RAISED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1