BEUDAMED
    FDA Recall Terminated

    Misys Laboratory, version 5.3 with Reference Laboratory Interface

    Recall: Z-0647-03 · Initiated October 18, 2002

    Recall

    Recall Number
    Z-0647-03
    Event Number
    25009
    Firm
    Sunquest Information Systems
    FEI Number
    1000306472
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    October 18, 2002
    Posted
    March 13, 2003
    Terminated
    December 3, 2004
    Address
    4801 E Broadway Blvd, Tucson, AZ, 85711

    Description

    Misys Laboratory, version 5.3 with Reference Laboratory Interface

    Reason

    Software anomaly, incorrect coding. Some comments were not transfered when coming from the Reference Laboratory Interface.

    Action

    A product workaround was communicated to the two affected sites by facsimile on October 18, 2002. The recall is complete.

    Distribution

    States of WI, and IL.

    Quantity

    2