BEUDAMED
    FDA Recall Terminated

    Misys Laboratory versions 5.2, 5.23, or 5.3 with ADT Interface to CoPathPlus.

    Recall: Z-0325-03 · Initiated October 24, 2002

    Recall

    Recall Number
    Z-0325-03
    Event Number
    25077
    Firm
    Sunquest Information Systems
    FEI Number
    1000306472
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    October 24, 2002
    Posted
    December 11, 2002
    Terminated
    February 26, 2013
    Address
    4801 E Broadway Blvd, Tucson, AZ, 85711

    Description

    Misys Laboratory versions 5.2, 5.23, or 5.3 with ADT Interface to CoPathPlus.

    Reason

    Interfacing software systems have inconsistent character recognition characteristics.

    Action

    A recall notice was sent to hospitals on October 24, 2002. It communicated a temporary procedure to work around the problem. Also mentioned was the availabllity of a utility to detect and report suspected duplicate Medical Record Numbers.

    Distribution

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

    Quantity

    190