BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 2050514 · Received April 5, 2011

    Report

    Report Number
    1824206-2011-02010
    Event Type
    Malfunction
    Date Received
    April 5, 2011
    Date of Event
    March 8, 2011
    Report Date
    March 8, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE SIDE RAIL WELDING BROKEN CAUSING SIDE RAILS NOT TO LATCH. THE TECHNICIAN REPLACED THE LEFT HEAD AND THE RIGHT FOOT SIDE RAILS TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    TECHNICIAN ALLEGED THAT THE LEFT HEAD AND THE RIGHT FOOT SIDE RAILS WOULD NOT LATCH. NO ALLEGED INJURIES BY ACCOUNT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1