BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE-

    MDR report key: 2253793 · Received August 10, 2011

    Report

    Report Number
    1824206-2011-04199
    Event Type
    Malfunction
    Date Received
    August 10, 2011
    Date of Event
    July 28, 2011
    Report Date
    July 28, 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 BED IN "DOWN" STORAGE. HEAD UP FUNCTION NOT WORKING. FUNCTION DOES NOT WORK MANUALLY OR UNDER POWER. BATTERY LED IS ON. DETERMINED THE PROBLEM TO BE FAULTY VALVE GUIDE TUBE. REPLACED HEAD UP VALVE GUIDE TUBE TO RESOLVE THIS ISSUE. BED FUNCTIONS PROPERLY.

    Description of Event or Problem · 1

    BED FOUND IN "DOWN" STORAGE. HEAD UP FUNCTION NOT WORKING. NO INJURY REPORTED.

    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