Misys Laboratory versions 5.2, 5.23, or 5.3 with ADT Interface to CoPathPlus.
FDA Recall Z-0325-03 · Posted 2002-12-11
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Recalling FirmSunquest Information Systems
Recall StatusTerminated
Product CodeJQP
Date Initiated2002-10-24
Date Terminated2013-02-26
Product Quantity190
Reason for Recall
Interfacing software systems have inconsistent character recognition characteristics.
Firm Action
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
Distribution Pattern
Nationwide and to Denmark, Bermuda, United Kingdom, Saudi Arabia, Canada.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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