Atlas FDA

Misys Laboratory System versions 5.23 and 5.3

FDA device recall Z-0804-03 · posted 2003-05-09 · Terminated

Recall details

Recalling firm
Misys Healthcare Systems
Reason for recall
Software anomaly.
Action taken
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.
Root cause
Other
Status
Terminated
Quantity affected
463
Distribution
Nationwide and to United Kingdom, Ireland, Canada, Denmark, Bermuda, Saudi Arabia, United Arab Emirates,
Date initiated
2003-03-27
Date posted
2003-05-09
Date terminated
2004-04-21
Location
Tucson, AZ

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.