Device recall
Z-0729-2007: Flexxus™ Endoscopic Biliary Stent, 7.5 Fr 10mm diameter x 40 mm length Item…
FDA device recall · Class II · Conmed Endoscopic Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0729-2007 |
|---|---|
| Recall event | 37628 |
| Product | Flexxus™ Endoscopic Biliary Stent, 7.5 Fr 10mm diameter x 40 mm length Item Number: LXB10040 |
| Product code | FGE |
| Recalling firm | Conmed Endoscopic Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2007 |
| 510(k) numbers | K031186 |
| FEI number | 1000159712 |
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