FDA Recall Terminated

Misys Laboratory System versions 5.23 and 5.3

Recall: Z-0804-03 · Initiated March 27, 2003

Recall

Recall Number
Z-0804-03
Event Number
25996
Firm
Misys Healthcare Systems
FEI Number
1000306472
Status
Terminated
Root Cause
Other
Initiated
March 27, 2003
Posted
May 9, 2003
Terminated
April 21, 2004
Address
4801 E Broadway Blvd, Tucson, AZ, 85711

Description

Misys Laboratory System versions 5.23 and 5.3

Reason

Software anomaly.

Action

The firm sent notification of the situation in Product Safety Notice PSN-03-L14 by fax on 3/27/2003. It communicated a workaround solution and informed of an impending code addition intended to be made available at a future date.

Distribution

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

Quantity

463