Atlas FDA

Misys Laboratory version 5.3

FDA device recall Z-0422-03 · posted 2003-01-11 · Terminated

Recall details

Recalling firm
Sunquest Information Systems
Reason for recall
Software development logic defect.
Action taken
Notice of the recall was sent to customers by fax on 11/15/2002.
Root cause
Other
Status
Terminated
Product code
JQP
Quantity affected
461
Distribution
Nationwide and to United Kingdom, Canada, Ireland, Denmark, Bermuda, Saudi Arabia, United Arab Emirates.
Date initiated
2002-11-15
Date posted
2003-01-11
Date terminated
2004-06-01
Location
Tucson, AZ

Monitor recalls programmatically

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