BEUDAMED
    FDA Recall Terminated

    Misys Laboratory System versions 5.2, 5.23 and 5.3

    Recall: Z-0626-03 · Initiated January 31, 2003

    Recall

    Recall Number
    Z-0626-03
    Event Number
    25557
    Firm
    Misys Healthcare Systems
    FEI Number
    1000306472
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    January 31, 2003
    Posted
    March 6, 2003
    Terminated
    July 14, 2004
    Address
    4801 E Broadway Blvd, Tucson, AZ, 85711

    Description

    Misys Laboratory System versions 5.2, 5.23 and 5.3

    Reason

    Software anomaly. Patient results may be filed in the incorrect patient file

    Action

    Notice of the correction was made by Fax on 1/31/2003. The notice indicated a procedural workaround to prevent the occurance of the defect. Corrections will be made to the software at only affected sites. These have been instructed to contact Applications Interface to schedule correction of the interface.

    Distribution

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

    Quantity

    542