Device recall
Z-0841-2013: Monaco RTP System. Radiation treatment planning.
FDA device recall · Class II · Elekta, Inc.
Key facts
| Recall number (Z-number) | Z-0841-2013 |
|---|---|
| Recall event | 64328 |
| Product | Monaco RTP System. Radiation treatment planning. |
| Product code | MUJ |
| Recalling firm | Elekta, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 21, 2014 |
| 510(k) numbers | K110730 |
| FEI number | 1037831 |
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