BEUDAMED
    FDA Enforcement Class II Terminated

    DxH 600 Coulter Cellular Analysis System, Catalog No. B23858

    Recall: Z-1014-2017 · Reported January 18, 2017

    Enforcement

    Recall Number
    Z-1014-2017
    Event ID
    76044
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Beckman Coulter Inc.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    January 18, 2017
    Initiation Date
    December 19, 2016
    Classification Date
    January 11, 2017
    Termination Date
    May 12, 2017
    Address
    250 S Kraemer Blvd, Brea, CA, 92821-6232, United States

    Description

    DxH 600 Coulter Cellular Analysis System, Catalog No. B23858

    Reason

    Beckman Coulter has determined that additional clarification for the Blast Suspect messages is necessary. In rare situations, the UniCel DxH 800 and DxH 600 Coulter Cellular Analysis System may not flag or detect blasts in some blood samples. This is due to limitations in the available technology as well as sample limitations.

    Code Info

    Serial Numbers: All

    Distribution

    Worldwide Distribution - USA (nationwide) Distribution including Puerto Rico and to the countries of : Australia, Belarus, Belgium, Bosnia and Herzegovina, Brunei Darussalam, Canada, China, Columbia, Croatia, Czech Republic, France, Germany, Gibraltar, Ecuador Hong Kong, India, Israel, Italy, Japan, Jordan, Korea, Kuwait, Lebanon, Macao, Malaysia, Mayotte, Mexico, Morocco, Myanmar, New Zealand, Oman, Panama, Philippines, Poland, Portugal, Qatar, Russian Federation, Saudi Arabia, Singapore, Slovakia, Spain, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Turkey, United Arab Republic, United Kingdom, Uruguay and Vietnam.

    Quantity

    1,282 units total (915 units in US)