BEUDAMED
    FDA Recall Terminated

    Misys Laboratory, GUI version 5.3

    Recall: Z-0495-03 · Initiated December 20, 2002

    Recall

    Recall Number
    Z-0495-03
    Event Number
    25378
    Firm
    Misys Healthcare Systems
    FEI Number
    1000306472
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    December 20, 2002
    Posted
    January 30, 2003
    Terminated
    December 1, 2004
    Address
    4801 E Broadway Blvd, Tucson, AZ, 85711

    Description

    Misys Laboratory, GUI version 5.3

    Reason

    An incorrect collection date and time may be accepted and filed to the patient file.

    Action

    The firm's recall notice was sent by fax to all customers on Jan. 3, 2003. It communicated a procedural workaround and the availability of product corrections.

    Distribution

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

    Quantity

    465