Device recall
Z-3211-2018: Ashland(TM) Box Film Ball Cube II EBT3, P/N: 027863-002 rev E Product is used to…
FDA device recall · Class II · Accuray Incorporated
Key facts
| Recall number (Z-number) | Z-3211-2018 |
|---|---|
| Recall event | 80933 |
| Product | Ashland(TM) Box Film Ball Cube II EBT3, P/N: 027863-002 rev E Product is used to calibrate CyberKnife systems |
| Product code | IYE |
| Recalling firm | Accuray Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 16, 2020 |
| FEI number | 3003873069 |
At a glance
- None 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