BEUDAMED
    FDA Recall Terminated

    Customized Automation Centrifuge, First and Second Generation.

    Recall: Z-0975-04 · Initiated May 6, 2004

    Recall

    Recall Number
    Z-0975-04
    Event Number
    29092
    Firm
    Beckman Coulter Inc
    FEI Number
    2050012
    Product Code
    JQC
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 6, 2004
    Posted
    July 20, 2004
    Terminated
    November 30, 2004
    Address
    200 S Kraemer Blvd, Brea, CA, 92822-6208

    Description

    Customized Automation Centrifuge, First and Second Generation.

    Reason

    Centrifuge loss of containment with potential for injury or exposure to biohazard among lab workers.

    Action

    Recall was by letter and by telephone. All customers have been contacted.

    Distribution

    Nationwide

    Quantity

    17