BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1900882 · Received November 9, 2010

    Report

    Report Number
    1824206-2010-10936
    Event Type
    Malfunction
    Date Received
    November 9, 2010
    Date of Event
    October 15, 2010
    Report Date
    October 15, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN INSPECTED HOSES AND CYLINDERS FOR LEAKS...NONE. THE TECHNICIAN WAS UNABLE TO RAISE THE HEAD SECTION MANUALLY. HE CHECKED VOLTAGE AT HEAD UP COIL...15VDC. THE TECHNICIAN REPLACED THE HEAD UP VALVE SOLENOID CARTRIDGE TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO REC'D INDICATES, THE HEAD OF THE BED WILL NOT RISE.

    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