VersaCell X3 Solution and VersaCell X3 Expansion Pack — Class III medical device recall Z-1832-2014
Terminated recall by Siemens Medical Solutions Diagnostics, reported 2014-06-25, distributed in IA, NY. The keyboard and monitor may not be properly secured to the monitor arm.
| Recall number | Z-1832-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions Diagnostics, Flanders, NJ, United States |
| Recall initiated | 2014-04-25 |
| Classified | 2014-06-19 |
| Reported by FDA | 2014-06-25 |
| Terminated | 2015-04-16 |
| Distributed | IA, NY |
| Countries outside the US | CA, CL, FR, GB, IN, IT, KR, MY, PE |
| Quantity | 19 units |
Product
VersaCell X3 Solution and VersaCell X3 Expansion Pack, a robotic laboratory sample-management system. It connects up to 3 instruments and provides a user interface that routes samples, reduces manual tasks and consolidates results.
Reason for recall
The keyboard and monitor may not be properly secured to the monitor arm.
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-1832-2014. 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.