Device recall
Z-1832-2014: VersaCell X3 Solution and VersaCell X3 Expansion Pack, a robotic laboratory…
FDA device recall · Class III · Siemens Medical Solutions Diagnostics
Key facts
| Recall number (Z-number) | Z-1832-2014 |
|---|---|
| Recall event | 68320 |
| 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. |
| Product code | LXG |
| Recalling firm | Siemens Medical Solutions Diagnostics |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 16, 2015 |
| 510(k) numbers | K970227 |
| FEI number | 1000122204 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database