BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 1112095 · Received August 6, 2008

    Report

    Report Number
    1824206-2008-03012
    Event Type
    Malfunction
    Date Received
    August 6, 2008
    Date of Event
    September 28, 2007
    Report Date
    September 28, 2007
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    HI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UPON COMPLAINT REVIEW IT WAS DETERMINED THAT IT IS A REPORTABLE EVENT FOR SIDERAIL NOT LATCHING. THE TECHNICIAN REPLACED SIDERAIL HARDWARE WHICH RESOLVED THE PROBLEM.

    Description of Event or Problem · 1

    THE BED'S RIGHT SIDE HEAD SIDERAIL WOULD NOT LOCK/LATCH IN THE UP POSITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P850 NA

    Patients

    Seq Age Sex Outcome Treatment
    1