BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2043420 · Received March 15, 2011

    Report

    Report Number
    1824206-2011-01568
    Event Type
    Malfunction
    Date Received
    March 15, 2011
    Date of Event
    February 23, 2011
    Report Date
    February 23, 2011
    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

    TECHNICIAN FOUND DURING FUNCTION CHECK THAT THE HEAD WILL NOT RAISE... CAUSE - CHECKED FOR LEAKS... NONE. TRIED TO RAISE MANUALLY... NO CHANGE. CHECKED VOLTAGE AT HEAD UP COIL... 15VDC. RESOLVE - REPLACED HEAD UP VALVE AND PERFORMED FUNCTION CHECK TO RESOLVE THIS ISSUE. BED WAS STORED ON 8TH FLOOR.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATED THAT DURING FUNCTION CHECK, NOTICED THAT THE HEAD WILL NOT RAISE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900

    Patients

    Seq Age Sex Outcome Treatment
    1