BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA 850 BED

    MDR report key: 1112098 · Received August 6, 2008

    Report

    Report Number
    1824206-2008-03040
    Event Type
    Malfunction
    Date Received
    August 6, 2008
    Date of Event
    October 31, 2007
    Report Date
    October 31, 2007
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UPON COMPLAINT REVIEW IT WAS DETERMINED THAT THE BRAKES NOT HOLDING/WORKING COULD LEAD TO UNINTENTIONAL MOVEMENT OF THE BED WHICH HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN REPLACED THE CASTERS IN ORDER TO RESOLVE THE PROBLEM.

    Description of Event or Problem · 1

    WHILE PERFORMING MAINTENANCE ON THIS BED, IT WAS FOUND THAT THE BRAKES WOULD NOT HOLD.

    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