Device recall
Z-2439-2015: PTW UNIDOS webline: 1) REF T10023, 2) REF T10022 and 3) REF T10023 Firmware…
FDA device recall · Class II · PTW-Freiburg
Key facts
| Recall number (Z-number) | Z-2439-2015 |
|---|---|
| Recall event | 71395 |
| Product | PTW UNIDOS webline: 1) REF T10023, 2) REF T10022 and 3) REF T10023 Firmware version 2.05. Dosimeter for radiation therapy, diagnostic radiology and health physics. |
| Product code | IYE |
| Recalling firm | PTW-Freiburg |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 31, 2017 |
| 510(k) numbers | K951764 |
| FEI number | 3007360740 |
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