Atlas FDA

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FDA device recall Z-0497-03 · posted 2003-01-30 · Terminated

Recall details

Recalling firm
Sunquest Information Systems
Reason for recall
Software system defect resulting in incomplete patient results information.
Action taken
Product Safety Notice, PSN-02-L31 will be faxed to all affected customers. The notice provides product users with a description of the problem, an effective workaround, and the estimated release of coding modifications to the software version impacted.
Root cause
Other
Status
Terminated
Product code
JQP
Quantity affected
30
Distribution
Nationwide
Date initiated
2002-12-06
Date posted
2003-01-30
Date terminated
2013-02-26
Location
Tucson, AZ

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