BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BACI/ALERT BLOOD CULTURE BOTTLE

    MDR report key: 89548 · Received May 7, 1997

    Report

    Report Number
    1039284-1997-00001
    Event Type
    Injury
    Date Received
    May 7, 1997
    Date of Event
    April 7, 1997
    Manufacturer
    ORGANON TEKNIKA CORP.
    Product Code
    MDB
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INDIVIDUAL WAS CUT BY A BROKEN BLOOD CULTURE BOTTLE WHEN TRYING TO REMOVE THE BOTTLE FROM AN INSTRUMENT. THE RIGHT INNER THUMB WAS CUT. THE EVENT HAPPENED ABOUT SIX AM AND THE INDIVIDUAL WENT TO THE EMERGENCY ROOM BECAUSE THE EMPLOYEE HEALTH DEPT WAS CLOSED. SHE WAS GIVEN A TETANUS SHOT. INDIVIDUAL RECEIVED HEPATITIS AND GAMMA GLOBULIN SHOTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BACI/ALERT BLOOD CULTURE BOTTLE MICROBIAL GROWTH MONITOR MDB ORGANON TEKNIKA CORP. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 35 YR Required Intervention