BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1952448 · Received January 3, 2011

    Report

    Report Number
    1824206-2011-00008
    Event Type
    Malfunction
    Date Received
    January 3, 2011
    Date of Event
    December 12, 2010
    Report Date
    December 12, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THAT AN UNK LIQUID HAD GOTTEN AROUND THE LATCH MECHANISM AND PARTIALLY DRIED CAUSING THE LATCH TO NOT MOVE FREELY. THE TECHNICIAN CLEANED THE LATCHING MECHANISM ALLOWING IT TO MOVE FREELY AND THE LEFT SIDE RAIL BEGAN LATCHING CORRECTLY.

    Description of Event or Problem · 1

    TECHNICIAN ALLEGED THAT THE LEFT SIDE RAIL IS NOT LATCHING CORRECTLY. NO PT IMPACT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1