Device recall
Z-0179-2008: Edwards Lifesciences LifeStent FlexStar Bilary Stent System Application, Model…
FDA device recall · Class II · Edwards Lifesciences, Llc
Key facts
| Recall number (Z-number) | Z-0179-2008 |
|---|---|
| Recall event | 45436 |
| Product | Edwards Lifesciences LifeStent FlexStar Bilary Stent System Application, Model EX080801CD; 8 MM x 80 MM stent, 80 CM Delivery System, Lot FR6K0319, Edwards Lifesciences, LLC., Irvine, CA 92614 |
| Product code | FGE |
| Recalling firm | Edwards Lifesciences, Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 26, 2012 |
| 510(k) numbers | K053404 |
| FEI number | 2015691 |
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