Device recall
Z-0713-2025: Sheath, 20 Fr., 130 mm (REF: WA2PS20S), gastroenterology-urology endoscopic…
FDA device recall · Class I · Trokamed GmbH
Key facts
| Recall number (Z-number) | Z-0713-2025 |
|---|---|
| Recall event | 95770 |
| Product | Sheath, 20 Fr., 130 mm (REF: WA2PS20S), gastroenterology-urology endoscopic access overtube. |
| Product code | FED |
| Recalling firm | Trokamed GmbH |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K200770 |
| FEI number | 3004595684 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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