Device recall
Z-0942-2022: ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0…
FDA device recall · Class II · Varian Medical Systems Imaging Laboratory GmbH
Key facts
| Recall number (Z-number) | Z-0942-2022 |
|---|---|
| Recall event | 89922 |
| Product | ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0, 16.1 |
| Product code | IYE |
| Recalling firm | Varian Medical Systems Imaging Laboratory GmbH |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K133572, K173838 |
| FEI number | 3003094912 |
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