BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AEROBIC BLOOD CULTURE BOTTLES

    MDR report key: 240484 · Received September 9, 1999

    Report

    Report Number
    1039284-1999-00001
    Event Type
    Injury
    Date Received
    September 9, 1999
    Date of Event
    July 30, 1999
    Report Date
    August 9, 1999
    Manufacturer
    ORGANON TEKNIKA CORP
    Product Code
    MDB
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INDEX FINGER ON THE LEFT HAND SUFFERED A CUT AFTER REMOVAL FROM INSTRUMENT, EVEN THOUGH TECH WAS WARNED OF CRACK IN BOTTLE. PNEUMATIC TUBES WITH MORE THAN ONE BOTTLE PER CARRIER ARE OFTEN USED FOR TRANSPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AEROBIC BLOOD CULTURE BOTTLES BACT/ALERT SYSTEM MDB ORGANON TEKNIKA CORP * 209331

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Required Intervention