BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1894059 · Received November 4, 2010

    Report

    Report Number
    1824206-2010-10868
    Event Type
    Malfunction
    Date Received
    November 4, 2010
    Date of Event
    October 11, 2010
    Report Date
    October 11, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE BED IS LEAKING FLUID FROM HI/LOW FOOT CYLINDER. REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE FOOT HI/LOW IS DRIFTING ON THIS BED, HE HAS CHANGED THE VALVE BUT THE ISSUE REMAINS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1