BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2182139 · Received June 23, 2011

    Report

    Report Number
    1824206-2011-03404
    Event Type
    Malfunction
    Date Received
    June 23, 2011
    Date of Event
    February 22, 2011
    Report Date
    February 22, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN INSPECTED AND CLEANED ALL OF THE SIDERAIL LATCHES AND ALL FOUR SIDERAILS WERE LATCHING PROPERLY.

    Description of Event or Problem · 1

    THE ACCOUNT STATED THE BED WAS ALARMING INTERMITTENTLY. SHE FOUND THE LEFT INTERMEDIATE SIDERAIL IS SOMETIMES HARD TO LATCH AND WHEN IT IS LATCHED, IT DOES LATCH PROPERLY AND STAY UP PROPERLY. SOMETIMES IT IS HARD TO GET LATCHED.

    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 UNK