BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2033127 · Received February 28, 2011

    Report

    Report Number
    1824206-2011-01132
    Event Type
    Malfunction
    Date Received
    February 28, 2011
    Date of Event
    February 10, 2011
    Report Date
    February 10, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT THERE WAS NO HEAD UP FUNCTION ON THE BED. CAUSE: VALVE S7 WAS NOT OPENING. REPLACED VALVE S7 TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT ALLEGED THAT THERE WAS NO HEAD UP FUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900F005769

    Patients

    Seq Age Sex Outcome Treatment
    1