Device recall
Z-1066-2012: Elekta Synergy XVI 4.5 and R4.6 To be used as part of radiation therapy…
FDA device recall · Class II · Elekta, Inc.
Key facts
| Recall number (Z-number) | Z-1066-2012 |
|---|---|
| Recall event | 61050 |
| Product | Elekta Synergy XVI 4.5 and R4.6 To be used as part of radiation therapy treatment process. |
| Product code | IYE |
| Recalling firm | Elekta, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2012 |
| 510(k) numbers | K100115 |
| 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