BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MICROLAB AT PLUS 2

    MDR report key: 422456 · Received October 6, 2002

    Report

    Report Number
    2915796-2002-00028
    Event Type
    Malfunction
    Date Received
    October 6, 2002
    Date of Event
    September 4, 2002
    Manufacturer
    HAMILTON BONADUZ AG
    Product Code
    JTC
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    HAMILTON CO WAS INFORMED ON 9/9/2002 OF AN EVENT THAT OCCURRED IN 2002, IN WHICH THE HAMILTON MICROLAB AT +2 INSTRUMENT REPORTEDLY ASPIRATED AND DISPENSED SAMPLE TWICE IN ROW H AND DID NOT GENERATE AN ERROR MESSAGE. NO DEATH OR INJURY RESULTED FROM THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MICROLAB AT PLUS 2 MICROTITER DILUTING/DISPENSING JTC HAMILTON BONADUZ AG NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other