Device recall
Z-1030-2011: Precise Treatment Table The Precise Treatment Table is intended as a universal…
FDA device recall · Class II · Elekta, Inc.
Key facts
| Recall number (Z-number) | Z-1030-2011 |
|---|---|
| Recall event | 57570 |
| Product | Precise Treatment Table The Precise Treatment Table is intended as a universal patient treatment support and positioning table for radiation therapy and simulation use. It is for use with existing Elekta Linear Accelerators and Simulators and adaptable to third party radiotherapy products. |
| Product code | JAI |
| Recalling firm | Elekta, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 9, 2012 |
| 510(k) numbers | K983678 |
| FEI number | 1037831 |
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