BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 2151342 · Received June 7, 2011

    Report

    Report Number
    1824206-2011-03107
    Event Type
    Malfunction
    Date Received
    June 7, 2011
    Date of Event
    May 16, 2011
    Report Date
    May 16, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    THE ACCOUNT'S MAINTENANCE ALLEGED, THE BRAKE IS NOT HOLDING WELL ON THE BED. THE BRAKE/STEER PEDAL COULD BE PLACED INTO THE BRAKE POSITION BUT THE BED WOULD STILL ROLL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 852

    Patients

    Seq Age Sex Outcome Treatment
    1