FDA Device recall Z-2263-2015
Paragon Laboratory Management
- FDA Device
- Class II
- terminated
- Published 2015-08-05
On 2015-08-05 the FDA classified a Class II recall of Paragon Laboratory Management by Mckesson Technologies, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2263-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-15 |
| Published | 2015-08-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Mckesson Technologies |
| Distribution | US |
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.
Identifiers
| code_info | Model 12.1 and 12.1.1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2263-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.