Recall Z-2263-2015— McKesson Technologies, Inc.

Name: FDA recall Z-2263-2015
Creator: U.S. Food and Drug Administration
Published: 2014-06-15

Class II · Terminated

Class II FDA medical device recall by McKesson Technologies, Inc., initiated 2014-06-15, terminated 2022-02-01. FDA's recall record names no specific 510(k) clearance for this event. Product: Paragon Laboratory Management. Reason: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with Microsoft SQL Server 2012, the Final Cumulative Report may incorrectly display the data..

Recalling firm: McKesson Technologies, Inc.
Classification: Class II
Status: Terminated
Initiated: 2014-06-15
Terminated: 2022-02-01
Firm location: Charlotte, NC, United States

Product description

Paragon Laboratory Management

Reason for recall

For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with Microsoft SQL Server 2012, the Final Cumulative Report may incorrectly display the data.

Data sourced from openFDA. This site is unofficial and independent of the FDA.