BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1934254 · Received December 3, 2010

    Report

    Report Number
    1824206-2010-11365
    Event Type
    Malfunction
    Date Received
    December 3, 2010
    Date of Event
    November 8, 2010
    Report Date
    November 8, 2010
    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

    THE TECHNICIAN FOUND THE FUNCTION DOES NOT WORK MANUALLY OR UNDER POWER AND THE BATTERY LED IS ON. THE TECHNICIAN DETERMINED THE PROBLEM TO BE A FAULTY VALVE GUIDE TUBE. THE TECHNICIAN REPLACED THE HEAD UP VALVE GUIDE TUBE TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFORMATION REC'D INDICATES THE HEAD UP FUNCTION IS NOT WORKING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1