BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    4 MOTOR ADVANCE BED

    MDR report key: 1811262 · Received August 11, 2010

    Report

    Report Number
    1824206-2010-09270
    Event Type
    Malfunction
    Date Received
    August 11, 2010
    Date of Event
    July 19, 2010
    Report Date
    July 19, 2010
    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 ACCOUNT REPLACED THE OPEN BED EXIT TAPE SWITCHES TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED WITH NO ONE IN THE BED HE CAN TURN THE BED EXIT SYSTEM ON AND THE LED FOR THE BED EXIT WILL ILLUMINATE BUT THE ALARM WILL NOT SOUND AFTER THE SECOND DELAY. THE ACCOUNT STATED WHEN HE UNPLUGS THE TAPE SWITCHES FROM THE BED, THE ALARM WILL THEN SOUND.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 4 MOTOR ADVANCE BED AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 1104

    Patients

    Seq Age Sex Outcome Treatment
    1