BEUDAMED
    FDA Recall Terminated

    Cannabinoids Intercept Micro Plate EIA 100 plate kit

    Recall: Z-0481-2009 · Initiated September 8, 2008

    Recall

    Recall Number
    Z-0481-2009
    Event Number
    49562
    Firm
    OraSure Technologies, Inc.
    FEI Number
    2528909
    Product Code
    LDJ
    Status
    Terminated
    Root Cause
    Other
    Initiated
    September 8, 2008
    Posted
    December 18, 2008
    Terminated
    December 18, 2008
    Address
    1745 Eaton Ave, Bethlehem, PA, 18018-1769

    Description

    Cannabinoids Intercept Micro Plate EIA 100 plate kit

    Reason

    Readings, high: intermittent high absorbance readings. For further information, please contact the firm at 610-882-1820.

    Action

    On 9/8/08, the recalling firm telephoned the customer to inform them of the problem. As a follow up to the telephone call, the recalling firm issued a recall letter dated 9/11/08 to the customer.

    Distribution

    The product was shipped to one customer in New York.

    Quantity

    1 kit