BEUDAMED
    FDA Recall Terminated

    Misys Laboratory System Versions 5.2, 5.23 and 5.3

    Recall: Z-0614-03 · Initiated January 31, 2003

    Recall

    Recall Number
    Z-0614-03
    Event Number
    25556
    Firm
    Misys Healthcare Systems
    FEI Number
    1000306472
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    January 31, 2003
    Posted
    March 6, 2003
    Terminated
    May 7, 2004
    Address
    4801 E Broadway Blvd, Tucson, AZ, 85711

    Description

    Misys Laboratory System Versions 5.2, 5.23 and 5.3

    Reason

    Software anomaly. Rejecting the selected Autofiling status may result in the change being accepted rather than rejected.

    Action

    Firm sent notice by FAX on 1/31/2003. A workaround provided should prevent the problem until a software fix is made available. Clients can expect a notice when this is made available.

    Distribution

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

    Quantity

    542