BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA 850 BED

    MDR report key: 1162722 · Received September 8, 2008

    Report

    Report Number
    1824206-2008-03332
    Event Type
    Malfunction
    Date Received
    September 8, 2008
    Date of Event
    August 13, 2008
    Report Date
    August 13, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE HI-LOW DRIFTING IS UNINTENTIONAL MOVEMENT OF THE BED WHICH HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN CLEANED AND LUBRICATED THE HI-LOW DRIVE IN ORDER TO RESOLVE THE PROBLEM. ALL BED DRIVES ARE REQUIRED TO BE INSPECTED, CLEANED, AND LUBRICATED AT LEAST ONCE A YEAR IN ACCORDANCE WITH THE PRODUCT SERVICE MANUAL.

    Description of Event or Problem · 1

    A TECHNICIAN DETERMINED THAT THIS BED WAS DRIFTING DOWN FROM THE HIGH POSITION. THERE WERE NO INJURIES IN THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA 850 BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P850 NA

    Patients

    Seq Age Sex Outcome Treatment
    1