Device recall
Z-0911-2011: Varian Medical Systems, Eclipse Client software versions with build numbers from…
FDA device recall · Class II · Varian Medical Systems, Palo Alto, CA
Key facts
| Recall number (Z-number) | Z-0911-2011 |
|---|---|
| Recall event | 56772 |
| Product | Varian Medical Systems, Eclipse Client software versions with build numbers from 7.3.10 through 8.6.15 (i.e. excluding 8.6.17); Model Number: H48; Radiation Treatment Planning System |
| Product code | MUJ |
| Recalling firm | Varian Medical Systems, Palo Alto, CA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 21, 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