BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIQUICHEK CARDIAC MARKERS CONTROL LT

    MDR report key: 547225 · Received October 5, 2004

    Report

    Report Number
    2016706-2004-00002
    Event Type
    Other
    Date Received
    October 5, 2004
    Date of Event
    August 28, 2004
    Report Date
    September 24, 2004
    Manufacturer
    BIO-RAD LABORATORIES
    Product Code
    JJT
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A LAB PROFESSIONAL SPLASHED LEVEL 2, CARDIAC MARKERS LT IN THEIR EYE. THE EVENT OCCURRED IN 2004 WHILE THE CUSTOMER WAS WORKING AT THEIR PART-TIME JOB.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIQUICHEK CARDIAC MARKERS CONTROL LT ENZYME CONTROLS (ASSAYED AND UNASSAYED) JJT BIO-RAD LABORATORIES NA 31132

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other