BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2033118 · Received February 28, 2011

    Report

    Report Number
    1824206-2011-01142
    Event Type
    Malfunction
    Date Received
    February 28, 2011
    Date of Event
    February 11, 2011
    Report Date
    February 13, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT THE HEAD SECTION OF BED WOULD NOT RAISE DUE TO PLUNGER FOR HEAD UP WAS SLIGHTLY RUSTED. REPLACED PLUNGER IN HEAD UP VALVE TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT ALLEGED THAT THE HEAD SECTION OF THE 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. PR1840A000001

    Patients

    Seq Age Sex Outcome Treatment
    1