BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2842277 · Received November 8, 2012

    Report

    Report Number
    1824206-2012-07271
    Event Type
    Malfunction
    Date Received
    November 8, 2012
    Date of Event
    February 22, 2012
    Report Date
    February 22, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN ISOLATED THE ISSUE TO THE FOOT HI/LOW VALVE. HE REPLACED THE FOOT HI/LOW VALVE TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE BED WILL NOT REMAIN LEVEL. THE FOOT HI/LOW FUNCTION IS DRIFTING DOWN A HALF AN INCH EVERY HOUR.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1