Device recall
Z-0916-04: Philips Pinnacle3 Version 6.4a Radiation Therapy Planning Software CD, Part…
FDA device recall · Class II · ADAC Laboratories
Key facts
| Recall number (Z-number) | Z-0916-04 |
|---|---|
| Recall event | 28478 |
| Product | Philips Pinnacle3 Version 6.4a Radiation Therapy Planning Software CD, Part Number 9104-0121B, Rev. A |
| 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