BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1840

    MDR report key: 3003445 · Received February 8, 2013

    Report

    Report Number
    1824206-2013-00944
    Event Type
    Malfunction
    Date Received
    February 8, 2013
    Date of Event
    January 19, 2013
    Report Date
    January 19, 2013
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    HE HILL-ROM TECHNICIAN FOUND THE CENTER ARM WAS BROKEN. HE REPLACED THE CENTER ARM TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATED THE RIGHT INTERMEDIATE SIDERAIL WOULD NOT LATCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    54019 1840 AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1840

    Patients

    Seq Age Sex Outcome Treatment
    1