BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    P850 CENTRA BED

    MDR report key: 1193481 · Received October 8, 2008

    Report

    Report Number
    1824206-2008-03738
    Event Type
    Malfunction
    Date Received
    October 8, 2008
    Date of Event
    September 9, 2008
    Report Date
    September 9, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE LOSS OF TRENDELENBURG/REVERSE TRENDELENBURG HAS THE POTENTIAL TO CAUSE SERIOUS INJURY OR DEATH. THE TECHNICIAN ADJUSTED THE TREND SWITCH IN ORDER TO RESOLVE THE PROBLEM.

    Description of Event or Problem · 1

    AN ACCOUNT STATED THAT THIS BED WOULD NOT GO INTO REVERSE TRENDELENBURG.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1