BEUDAMED
    FDA Recall Terminated

    Misys Commercial Laboratory version 2.x thru 3.4.1

    Recall: Z-0920-03 · Initiated April 1, 2003

    Recall

    Recall Number
    Z-0920-03
    Event Number
    26266
    Firm
    Misys Healthcare Systems
    FEI Number
    1000306472
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    April 1, 2003
    Posted
    June 5, 2003
    Terminated
    April 21, 2004
    Address
    4801 E Broadway Blvd, Tucson, AZ, 85711

    Description

    Misys Commercial Laboratory version 2.x thru 3.4.1

    Reason

    Urgent care STAT reports are not printing in a timely fashion.

    Action

    Recall notifications were sent to users on April 1, 2003 in Product Safety Notice PSN-03-L16 by facsimile.

    Distribution

    Nationwide and to Canada.

    Quantity

    109