Device recall
Z-0821-2015: VERO Linear Accelerator System, Model Number MHI-TM2000, MHI Identifier…
FDA device recall · Class II · MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK
Key facts
| Recall number (Z-number) | Z-0821-2015 |
|---|---|
| Recall event | 69825 |
| Product | VERO Linear Accelerator System, Model Number MHI-TM2000, MHI Identifier M101-14021, Software Version: 3.1, 3.2 and 3.5.0. |
| Product code | IYE |
| Recalling firm | MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 26, 2017 |
| 510(k) numbers | K072047, K122450 |
| FEI number | 3006942329 |
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