Device recall
Z-0206-2013: Pinnacle3 VCC P/N 4598 001 41341 REV A, Philips Medical Systems (Cleveland)…
FDA device recall · Class II · Philips Medical Systems (Cleveland), Inc.
Key facts
| Recall number (Z-number) | Z-0206-2013 |
|---|---|
| Recall event | 63430 |
| Product | Pinnacle3 VCC P/N 4598 001 41341 REV A, Philips Medical Systems (Cleveland), Inc., Fitchburg, WI. Pinnacle3 Radiation Therapy Planning System is a computer software package intended to provide support for radiation therapy treatment planning for the treatment of benign or malignant disease… |
| Product code | IYE |
| Recalling firm | Philips Medical Systems (Cleveland), Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 21, 2013 |
| 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