Paragon Laboratory Management
FDA device recall Z-2263-2015 · posted 2015-07-27 · Terminated
Recall details
- Recalling firm
- McKesson Technologies, Inc.
- 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.
- Action taken
- McKesson issued a Clinical Alert to notify customers of the issue on June 15, 2015, and requested that customers disable Cumulative Reporting. McKesson is identifying customers currently in a live environment with Microsoft SQL Server 2012 and the affected configuration. McKesson will provide those customers with corrective software, and provide assistance in generating correct reports and updating those to the patient folder. For further questions, please call (404) 338-3556.
- Root cause
- Software design
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 128
- Distribution
- 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
- Date initiated
- 2014-06-15
- Date posted
- 2015-07-27
- Date terminated
- 2022-02-01
- Location
- Charlotte, NC
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