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Z-2263-2015 Class II Terminated

Recalled by McKesson Technologies, Inc. — Charlotte, NC

FDA device recall Z-2263-2015 was initiated by McKesson Technologies, Inc. on June 15, 2014 and is designated Class II. 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. The recall status is terminated (terminated February 1, 2022). Affected quantity: 128.

Recall Details

Product Type: Devices
Report Date: August 5, 2015
Initiation Date: June 15, 2014
Termination Date: February 1, 2022
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 128

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.

Distribution Pattern

Nationwide Distribution including Puerto Rico and to the states of : CA, CO., CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NH, NJ, NM, NY, NC, OH, OK, OA, PA, SC, SD, TN, TX, VT, VA, WV and WY.

Code Information

Model 12.1 and 12.1.1