BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 1944814 · Received December 10, 2010

    Report

    Report Number
    1824206-2010-11501
    Event Type
    Malfunction
    Date Received
    December 10, 2010
    Date of Event
    November 15, 2010
    Report Date
    November 15, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE BED EXIT TAPE STRIP NOT FUNCTIONING. HE REPLACED THE TAPE STRIP TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE BED EXIT ALARM IS NOT SOUNDING WHEN THE PATIENT COMES OUT OF THE BED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 850

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK