Device recall
Z-2622-2011: Interplant Radiation Treatment Planning System, Interplant Release 3.4.0 Used…
FDA device recall · Class II · Computerized Medical Systems Inc
Key facts
| Recall number (Z-number) | Z-2622-2011 |
|---|---|
| Recall event | 58228 |
| Product | Interplant Radiation Treatment Planning System, Interplant Release 3.4.0 Used when planning and performing prostate brachytherapy implant procedure. It provides ultrasound probe alignment and radioactive seed implantation. |
| Product code | MUJ |
| Recalling firm | Computerized Medical Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 4, 2013 |
| 510(k) numbers | K982696 |
| FEI number | 1937649 |
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