BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1961312 · Received December 20, 2010

    Report

    Report Number
    1824206-2010-11785
    Event Type
    Malfunction
    Date Received
    December 20, 2010
    Date of Event
    November 24, 2010
    Report Date
    November 24, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN INSPECTED THE BED IN THE MAINTENANCE AREA COMPLETELY AND DID FIND THAT THE HI-LO HEAD DOWN HYDRAULIC VALVE WAS BAD. HE REPLACED THE HI-LO HEAD DOWN HYDRAULIC VALVE TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD HI/LOW FUNCTION IS DRIFTING DOWN.

    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