BEUDAMED
    FDA Adverse Event Other Summary report: N

    MULTICAP CAPILLARY TUBES

    MDR report key: 527724 · Received February 20, 2004

    Report

    Report Number
    1217157-2004-00001
    Event Type
    Other
    Date Received
    February 20, 2004
    Date of Event
    January 11, 2004
    Report Date
    February 20, 2004
    Manufacturer
    BAYER CORP.
    Product Code
    GIO
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    TWO CUTS HAVE BEEN SUSTAINED BY BROKEN TUBES WHILE CAPPING THE TUBES WHICH EXPOSED THE OPERATOR TO PT BLOOD. THE BLOOD WITHIN THE CAPILLARY WAS NOT SUSPECTED TO HAVE INFECTED OPERATORS WITH ANY DESEASE, HOWEVER, BOTH OPERATORS ARE BEING CHECKED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MULTICAP CAPILLARY TUBES LITHIUM HEPARINIZED MICRO CAPILLARY TUBES GIO BAYER CORP. NA 0709221

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other