BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BACT/ALERT MEDIA CULTURE BOTTLE

    MDR report key: 496460 · Received November 18, 2003

    Report

    Report Number
    1039284-2003-00010
    Event Type
    Injury
    Date Received
    November 18, 2003
    Date of Event
    August 22, 2003
    Report Date
    November 10, 2003
    Manufacturer
    BIOMERIEUX, INC.
    Product Code
    JTA
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    A CUSTOMER WAS TRYING TO REMOVE A BACT/ALERT GLASS BOTTLE FROM THE BACT/ALERT 3D INSTRUMENT WHEN THE BOTTLE BROKE AND CUT THE FINGER OF THE CUSTOMER. THE BLEEDING WAS STOPPED. NO OTHER TREATMENT WAS GIVEN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BACT/ALERT MEDIA CULTURE BOTTLE MICROBIAL GROWTH MONITOR JTA BIOMERIEUX, INC. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other