Device recall
Z-0912-04: Pinnacle3 Radiation Therapy Planning System, Version 6.6c Kit, Model Number…
FDA device recall · Class II · ADAC Laboratories
Key facts
| Recall number (Z-number) | Z-0912-04 |
|---|---|
| Recall event | 28478 |
| Product | Pinnacle3 Radiation Therapy Planning System, Version 6.6c Kit, Model Number 9200-0613C-ENG |
| Product code | MUJ |
| Recalling firm | ADAC Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 1, 2005 |
| FEI number | 3004022368 |
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