BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CCU BED

    MDR report key: 2241333 · Received September 2, 2011

    Report

    Report Number
    1824206-2011-04624
    Event Type
    Malfunction
    Date Received
    September 2, 2011
    Date of Event
    August 22, 2011
    Report Date
    August 22, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH FOUND A LOT OF PLAY IN THE HEX RODS AND ROCKER ARMS. HE ADJUSTED THE HEX RODS AND ROCKER ARMS TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE BRAKES WERE HARD TO SET AND THE HEAD END BRAKE CASTERS DID NOT HOLD IN THE BRAKE MODE WHEN SET FROM THE FOOT END OF THE BED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CCU BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 894

    Patients

    Seq Age Sex Outcome Treatment
    1