BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE-

    MDR report key: 2142630 · Received June 21, 2011

    Report

    Report Number
    1824206-2011-03358
    Event Type
    Malfunction
    Date Received
    June 21, 2011
    Date of Event
    June 3, 2011
    Report Date
    June 3, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THE BED IN STORAGE AREA. HEAD SECTION WOULD NOT GO UP DUE TO BAD SOLENOID VALVE. REPLACED THE VALVE SOLENOID TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    BED IN STORAGE - CAUSE OF PROBLEM UNK. NO INJURY ALLEGED.

    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