McKesson Technologies, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2263-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Paragon Laboratory Management

Product Classification:

Class II

Date Initiated: June 15, 2014

Date Posted: August 5, 2015

Recall Number: Z-2263-2015

Event ID: 71570

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.

Status: Terminated

Product Quantity: 128

Code Information:

Model 12.1 and 12.1.1

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.

Voluntary or Mandated:

Voluntary: Firm initiated