BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MULTICAP CAPILLARY TUBES

    MDR report key: 534412 · Received March 16, 2004

    Report

    Report Number
    1217157-2004-00003
    Event Type
    Injury
    Date Received
    March 16, 2004
    Date of Event
    March 4, 2004
    Report Date
    March 15, 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

    OPERATOR EXPOSED TO PT BLOOD WHILE CAPPING MICROCAPILLARY TUBES. OPERATOR HAS BEEN TREATED PER HOSPITAL PROTOCOL.

    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