BEUDAMED
    FDA Recall Terminated

    Misys Laboratory System, version 5.3

    Recall: Z-0926-03 · Initiated May 13, 2003

    Recall

    Recall Number
    Z-0926-03
    Event Number
    26364
    Firm
    Misys Healthcare Systems
    FEI Number
    1000306472
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 13, 2003
    Posted
    June 17, 2003
    Terminated
    April 23, 2004
    Address
    4801 E Broadway Blvd, Tucson, AZ, 85711

    Description

    Misys Laboratory System, version 5.3

    Reason

    Two clients reported Quality Assurance dates could not be entered after 5/19/03.

    Action

    Product Safety Notice number PSN-03-L24 was issued on May 13, 2003 to all affected customers. It contained an effective workaround and communicated that the software fix was available and also included that for those clients that wanted to install it. Clients are reminded to return acknowledgement cards included in the mailing.

    Distribution

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

    Quantity

    466