Device recall
Z-0014-2009: Mobetron Model 1000, mobile electron linear accelerator, a device system which…
FDA device recall · Class II · Intraop Medical Corporation
Key facts
| Recall number (Z-number) | Z-0014-2009 |
|---|---|
| Recall event | 49022 |
| Product | Mobetron Model 1000, mobile electron linear accelerator, a device system which delivers radiation to an intraoperative site. |
| Product code | LHN |
| Recalling firm | Intraop Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 5, 2011 |
| 510(k) numbers | K981112 |
| FEI number | 3001874253 |
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