Atlas FDA

Misys Laboratory versions 5.23 and 5.3

FDA device recall Z-0423-03 · posted 2003-01-11 · Terminated

Recall details

Recalling firm
Sunquest Information Systems
Reason for recall
Software anomally.
Action taken
A recall notice along witn instructions for avoiding conditions that might cause the observed anomalous results was faxed to all customers 11/22/2002.
Root cause
Other
Status
Terminated
Quantity affected
623
Distribution
Nationwide and to the United Kingdom, Ireland, Canada, Denmark, Bermuda, Saudi Arabia, United Arab Emirates,
Date initiated
2002-11-22
Date posted
2003-01-11
Date terminated
2003-06-23
Location
Tucson, AZ

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