Device recall
Z-1578-05: Bard Luminexx Endoscopic Biliary Stent and Delivery System, 7.5 FR, 8 mm x 80…
FDA device recall · Class II · Angiomed Gmbh
Key facts
| Recall number (Z-number) | Z-1578-05 |
|---|---|
| Recall event | 32853 |
| Product | Bard Luminexx Endoscopic Biliary Stent and Delivery System, 7.5 FR , 8 mm x 80 mm Catalog Number: LXB08080 |
| Product code | FGE |
| Recalling firm | Angiomed Gmbh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 2, 2006 |
| FEI number | 3002806368 |
At a glance
- None 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