BEUDAMED
    FDA Recall Terminated

    Misys Laboratory version 5.3

    Recall: Z-0686-03 · Initiated February 28, 2003

    Recall

    Recall Number
    Z-0686-03
    Event Number
    25797
    Firm
    Misys Healthcare Systems
    FEI Number
    1000306472
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    February 28, 2003
    Posted
    April 2, 2003
    Terminated
    June 2, 2004
    Address
    4801 E Broadway Blvd, Tucson, AZ, 85711

    Description

    Misys Laboratory version 5.3

    Reason

    Patient results do not update properly when modified using on-line entry function.

    Action

    Product Safety Notice (PSN-03-L10) was sent to all affected clients by fax on 2/28/2003. It contained a procedural workaround. An announcement of the availability of a software upgrade or fix will be made when it is available.

    Distribution

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

    Quantity

    460