Paragon Laboratory Management — Class II medical device recall Z-2263-2015
Terminated recall by McKesson Technologies, Inc., reported 2015-08-05, distributed nationwide. For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with Microsoft SQL Server 2012, the Final
| Recall number | Z-2263-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | McKesson Technologies, Inc., Charlotte, NC, United States |
| Recall initiated | 2014-06-15 |
| Classified | 2015-07-27 |
| Reported by FDA | 2015-08-05 |
| Terminated | 2022-02-01 |
| Distributed | Nationwide (US) |
| Quantity | 128 |
| Model numbers | 12.1, 12.1.1 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2263-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.