BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MICROLAB AT PLUS 2

    MDR report key: 1306243 · Received January 7, 2009

    Report

    Report Number
    2250051-2008-80594
    Event Type
    Malfunction
    Date Received
    January 7, 2009
    Date of Event
    December 16, 2008
    Report Date
    January 7, 2009
    Manufacturer
    HAMILTON BONADUZ AG
    Product Code
    JTC
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    AL, US
    Reporter Occupation
    MEDICAL TECHNOLOGIST

    Narratives

    Description of Event or Problem · 1

    THE HAMILTON MICROLAB AT PLUS 2 INSTRUMENT DID NOT PIPETTE SAMPLE AND DILUENT AND DID NOT GENERATE AN ERROR MESSAGE. NO DEATH OR SERIOUS INJURY WAS ASSOCIATED WITH THIS INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MICROLAB AT PLUS 2 SAMPLE PIPETTER JTC HAMILTON BONADUZ AG 142036 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *