Device recall
Z-0821-2011: Varian brand Trilogy System with RapidArc, Model Numbers: H14, H26, H27, H29…
FDA device recall · Class II · Varian Medical Systems Inc.
Key facts
| Recall number (Z-number) | Z-0821-2011 |
|---|---|
| Recall event | 56774 |
| Product | Varian brand Trilogy System with RapidArc, Model Numbers: H14, H26, H27, H29; Distributed and Manufactured by: Varian Medical Systems Inc., Palo Alto, CA |
| Product code | IYE |
| Recalling firm | Varian Medical Systems Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 18, 2011 |
| 510(k) numbers | K072916 |
| FEI number | 2916710 |
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