Atlas FDA

Misys Laboratory versions 5.2, 5.23, or 5.3 with ADT Interface to CoPathPlus.

FDA device recall Z-0325-03 · posted 2002-12-11 · Terminated

Recall details

Recalling firm
Sunquest Information Systems
Reason for recall
Interfacing software systems have inconsistent character recognition characteristics.
Action taken
A recall notice was sent to hospitals on October 24, 2002. It communicated a temporary procedure to work around the problem. Also mentioned was the availabllity of a utility to detect and report suspected duplicate Medical Record Numbers.
Root cause
Other
Status
Terminated
Product code
JQP
Quantity affected
190
Distribution
Nationwide and to Denmark, Bermuda, United Kingdom, Saudi Arabia, Canada.
Date initiated
2002-10-24
Date posted
2002-12-11
Date terminated
2013-02-26
Location
Tucson, AZ

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