BEUDAMED
    FDA Recall Terminated

    Paragon Laboratory Management

    Recall: Z-2263-2015 · Initiated June 15, 2014

    Recall

    Recall Number
    Z-2263-2015
    Event Number
    71570
    Firm
    McKesson Technologies, Inc.
    FEI Number
    3010034769
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Software design
    Initiated
    June 15, 2014
    Posted
    July 27, 2015
    Terminated
    February 1, 2022
    Address
    10735 David Taylor Dr, Ste 100, Charlotte, NC, 28262-1288

    Description

    Paragon Laboratory Management

    Reason

    For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with Microsoft SQL Server 2012, the Final Cumulative Report may incorrectly display the data.

    Action

    McKesson issued a Clinical Alert to notify customers of the issue on June 15, 2015, and requested that customers disable Cumulative Reporting. McKesson is identifying customers currently in a live environment with Microsoft SQL Server 2012 and the affected configuration. McKesson will provide those customers with corrective software, and provide assistance in generating correct reports and updating those to the patient folder. For further questions, please call (404) 338-3556.

    Distribution

    Nationwide Distribution including Puerto Rico and to the states of : CA, CO., CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NH, NJ, NM, NY, NC, OH, OK, OA, PA, SC, SD, TN, TX, VT, VA, WV and WY.

    Quantity

    128