Atlas FDA

Misys Commercial Laboratory version 2.x thru 3.4.1

FDA device recall Z-0920-03 · posted 2003-06-05 · Terminated

Recall details

Recalling firm
Misys Healthcare Systems
Reason for recall
Urgent care STAT reports are not printing in a timely fashion.
Action taken
Recall notifications were sent to users on April 1, 2003 in Product Safety Notice PSN-03-L16 by facsimile.
Root cause
Other
Status
Terminated
Product code
JQP
Quantity affected
109
Distribution
Nationwide and to Canada.
Date initiated
2003-04-01
Date posted
2003-06-05
Date terminated
2004-04-21
Location
Tucson, AZ

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