Device recall
Z-0907-2011: ARTISTE and ONCOR Digital Linear Accelerators configured with the 160 leaf…
FDA device recall · Class II · Siemens Medical Solutions, Oncology Care Systems, 4040 Nelson Ave., Concord, CA 94510
Key facts
| Recall number (Z-number) | Z-0907-2011 |
|---|---|
| Recall event | 56773 |
| Product | ARTISTE and ONCOR Digital Linear Accelerators configured with the 160 leaf Multi-Leaf Collimator (MLC) and MEVATRON and PRIMUS Digital Linear Accelerators configured with the High Performance Defining Collimator (HPD); Product is manufactured by Kemnath, Germany-Siemens AG OCS and Siemens AG… |
| Product code | IYE |
| Recalling firm | Siemens Medical Solutions, Oncology Care Systems, 4040 Nelson Ave., Concord, CA 94510 |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 31, 2012 |
| FEI number | 2937457 |
At a glance
- None 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