BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CBC II

    MDR report key: 382048 · Received March 13, 2002

    Report

    Report Number
    2648666-2002-00003
    Event Type
    Injury
    Date Received
    March 13, 2002
    Date of Event
    February 13, 2002
    Report Date
    February 13, 2002
    Manufacturer
    STRYKER INSTRUMENTS
    Product Code
    CAC
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PER CUSTOMER: AN INDIVIDUAL UNIT WOULD NOT REINFUSE BLOOD BACK INTO THE PATIENT. UNIT DISPOSED OF.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CBC II AUTO TRANSFUSION APPARATUS CAC STRYKER INSTRUMENTS 0225-028-614 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention