Device recall
Z-1259-2008: Edwards LifeStent FlexStar Biliary Stent System; Biliary catheter and…
FDA device recall · Class II · Edwards Lifesciences, Llc
Key facts
| Recall number (Z-number) | Z-1259-2008 |
|---|---|
| Recall event | 46679 |
| Product | Edwards LifeStent FlexStar Biliary Stent System; Biliary catheter and accessories; Model Number: EX060303CD; Edwards Lifesciences LLC, Irvine, CA 92614. |
| Product code | FGE |
| Recalling firm | Edwards Lifesciences, Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 11, 2012 |
| 510(k) numbers | K053404 |
| FEI number | 2015691 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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