BEUDAMED
    FDA Recall Terminated

    Misys Laboratory System versions 5.2, 5.23, 5.3, 5.3.1 and 5.3.2.

    Recall: Z-0867-03 · Initiated April 14, 2003

    Recall

    Recall Number
    Z-0867-03
    Event Number
    26135
    Firm
    Misys Healthcare Systems
    FEI Number
    1000306472
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    April 14, 2003
    Posted
    May 29, 2003
    Terminated
    April 21, 2004
    Address
    4801 E Broadway Blvd, Tucson, AZ, 85711

    Description

    Misys Laboratory System versions 5.2, 5.23, 5.3, 5.3.1 and 5.3.2.

    Reason

    Incorrect results could be filed.

    Action

    The firm sent Product Safety Notice PSN-03-L18 by fax to customers on 4/14/2003.

    Distribution

    Nationwide and to Ireland, Canada, Denmark, United Kingdom, Saudi Arabia, United Arab Emirates.

    Quantity

    193