BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2091098 · Received May 12, 2011

    Report

    Report Number
    1824206-2011-02640
    Event Type
    Malfunction
    Date Received
    May 12, 2011
    Date of Event
    April 18, 2011
    Report Date
    April 18, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN SUPPORT TOLD THE ACCOUNT THAT A VALVE COULD BE STICKING INTERMITTENTLY. MAINTENANCE REPLACED THE HEAD DOWN VALVE AND THE PROBLEM RETURNED. REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    A NURSE TOLD THE ACCOUNTS MAINTENANCE THAT THE HEAD SECTION OF THE BED DRIFTED DOWN OVER NIGHT. MAINTENANCE COULD NOT GET THE BED TO DRIFT.

    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