BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA 850 BED

    MDR report key: 1112090 · Received August 6, 2008

    Report

    Report Number
    1824206-2008-03044
    Event Type
    Malfunction
    Date Received
    August 6, 2008
    Date of Event
    October 11, 2007
    Report Date
    October 11, 2007
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UPON COMPLAINT REVIEW, IT WAS DETERMINED THAT THIS TYPE OF FAILURE HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN REPLACED THE POWER CORD, IN ORDER TO RESOLVE THE PROBLEM.

    Description of Event or Problem · 1

    DURING PREVENTATIVE MAINTENANCE, IT WAS DETERMINED THAT THE AC POWER CORD WAS DAMAGED ON THIS BED.

    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