BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2000044 · Received February 3, 2011

    Report

    Report Number
    1824206-2011-00635
    Event Type
    Malfunction
    Date Received
    February 3, 2011
    Date of Event
    January 21, 2011
    Report Date
    January 21, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THE HEAD OF THE BED WOULD NOT RAISE. REMOVED THE SOLENOID - CLEANED AND RETESTED. HEAD WOULD STILL NOT RAISE. REPLACED SOLENOID HEAD UP TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT ALLEGED THAT THE HEAD OF BED WOULD NOT RAISE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1840RE200

    Patients

    Seq Age Sex Outcome Treatment
    1