Device recall
Z-1612-2008: Eclipse Treatment Planning System, Client 8.1.18 and DCF 8.1.17, model number…
FDA device recall · Class II · Varian Medical Systems Oncology Systems
Key facts
| Recall number (Z-number) | Z-1612-2008 |
|---|---|
| Recall event | 46902 |
| Product | Eclipse Treatment Planning System, Client 8.1.18 and DCF 8.1.17, model number H48 |
| Product code | MUJ |
| Recalling firm | Varian Medical Systems Oncology Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 17, 2011 |
| 510(k) numbers | K071873 |
| FEI number | 2916710 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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