BEUDAMED
    FDA Recall Terminated

    ARCHITECT Processing Module, manufactured by Abbott Laboratories, Irving, Texas

    Recall: Z-0172-04 · Initiated May 8, 2002

    Recall

    Recall Number
    Z-0172-04
    Event Number
    27180
    Firm
    Abbott Laboratories, Inc
    FEI Number
    1628664
    Product Code
    JJE
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 8, 2002
    Posted
    July 20, 2004
    Terminated
    November 26, 2003
    Address
    1921 Hurd Drive PO Box 152020, Irving, TX, 75015-2020

    Description

    ARCHITECT Processing Module, manufactured by Abbott Laboratories, Irving, Texas

    Reason

    If the interlock cable connected to the door lid sensor is disconnected or fails, the lid is detected as closed even though it may be open.

    Action

    Firm sent technical service bulletins with corrective instructions to consignees with all existing ARCHITECT i 2000 processing modules in February 2003.

    Distribution

    States of Virginia, Illinois, New York, Texas, Oklahoma, Pennsylvania, ILlinois, Michigan, California, New Hampshire, Ohio, Florida, Maryland, Nevada, Georgia, Minnesota, Colorado, Arizona, Missouri, Louisiana, Oregon, Wisconsin, Hawaii, Connecticut, New Hampshire, Massachusetts, Washington, South Carolina, Mississippi, Alabama, and Tennessee, and the following foreign countries: Austria, Denmark, Germany, Italy, Poland, South Africa, Sweden, England, Colombia, Australia, Japan, New Zealand, Belgium, Finland, Greece, Netherlands, Portugal, Romania, Turkey, Canada, Mexico, Hong Kong, Korea, Taiwan, Czech Republic, France, Israel, Norway, Saudi Arabia, Spain, United Arab Emirates, Brazil, Venezuela, India, Malaysia, and Thailand.

    Quantity

    1,167 units worldwide