Device recall
Z-1212-2007: The Pinnacle3 Radiation Therapy Planning (RTP) system and its associated…
FDA device recall · Class II · Philips Nuclear Medicine, Inc.
Key facts
| Recall number (Z-number) | Z-1212-2007 |
|---|---|
| Recall event | 39420 |
| Product | The Pinnacle3 Radiation Therapy Planning (RTP) system and its associated software; composed of several modules including the core Pinnacle3 functionality, Syntegra (TM), P3IMRT, P3MD and AcQSim3 (TM). The Pinnacle3 RTP system is composed of a Sun UNIX workstation (or UNIX-complaint computer) running… |
| Product code | MUJ |
| Recalling firm | Philips Nuclear Medicine, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 17, 2011 |
| 510(k) numbers | K041577 |
| FEI number | 3004022368 |
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