FDA Device recall Z-1832-2014
VersaCell X3 Solution and VersaCell X3 Expansion Pack, a robotic laboratory sample-management system
- FDA Device
- Class III
- terminated
- Published 2014-06-25
On 2014-06-25 the FDA classified a Class III recall of VersaCell X3 Solution and VersaCell X3 Expansion Pack, a robotic laboratory sample-management system by Siemens Medical Solutions Diagnostics, citing the keyboard and monitor may not be properly secured to the monitor arm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1832-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-04-25 |
| Published | 2014-06-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Diagnostics |
| Distribution | IA, NY |
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
The keyboard and monitor may not be properly secured to the monitor arm.
Identifiers
| code_info | Siemens Material Numbers: Instrument 10793839, Expansion Pack 10913528 |
|---|
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-1832-2014%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.