BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CCU BED

    MDR report key: 1122219 · Received August 15, 2008

    Report

    Report Number
    1824206-2008-03134
    Event Type
    Malfunction
    Date Received
    August 15, 2008
    Date of Event
    July 17, 2008
    Report Date
    July 17, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE SCALE WEIGHING INACCURATELY HAS THE POTENTIAL TO CAUSE SERIOUS INJURY OR DEATH. THE TECHNICIAN REPLACED THE LEFT FOOT LOAD BEAM IN ORDER TO RESOLVE THE PROBLEM.

    Description of Event or Problem · 1

    AN ACCOUNT REPORTED THAT THE SCALE ON THE BED WAS WEIGHING INACCURATELY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CCU BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P894 NA

    Patients

    Seq Age Sex Outcome Treatment
    1