Atlas FDA

Misys Laboratory, version 5.3 with Reference Laboratory Interface

FDA device recall Z-0647-03 · posted 2003-03-13 · Terminated

Recall details

Recalling firm
Sunquest Information Systems
Reason for recall
Software anomaly, incorrect coding. Some comments were not transfered when coming from the Reference Laboratory Interface.
Action taken
A product workaround was communicated to the two affected sites by facsimile on October 18, 2002. The recall is complete.
Root cause
Other
Status
Terminated
Product code
JQP
Quantity affected
2
Distribution
States of WI, and IL.
Date initiated
2002-10-18
Date posted
2003-03-13
Date terminated
2004-12-03
Location
Tucson, AZ

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