BEUDAMED
    FDA Recall Terminated

    Immulite 1000 CEA Catalog No. LKCE1

    Recall: Z-0972-04 · Initiated May 3, 2004

    Recall

    Recall Number
    Z-0972-04
    Event Number
    29084
    Firm
    Diagnostic Products Corp
    FEI Number
    3005250747
    Product Code
    DHX
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 3, 2004
    Posted
    July 20, 2004
    Terminated
    July 1, 2004
    Address
    5700 W 96th St, Los Angeles, CA, 90045-5544

    Description

    Immulite 1000 CEA Catalog No. LKCE1

    Reason

    Instabililty

    Action

    Notice was made via email or telephone. Users are to discard kits.

    Quantity

    884