Device recall
Z-0789-03: Medtronic AVE brand BridgeAssurant Balloon Expandable Stent Delivery System for…
FDA device recall · Class II · Medtronic Ave Inc
Key facts
| Recall number (Z-number) | Z-0789-03 |
|---|---|
| Recall event | 25794 |
| Product | Medtronic AVE brand BridgeAssurant Balloon Expandable Stent Delivery System for Biliary Catheter;Model #s: FB720VF, FB730 VF, FB740 VF, FB760 VF, FB820VF, FB830VF, FB840VF, FB860VF; FB720VL, FB730VL, FB820VL, FB830VL; FB720F, FB730F, FB740F, FB760F, FB820F, FB830F, FB840F, FB860F; FB720L, FB730L… |
| Product code | FGE |
| Recalling firm | Medtronic Ave Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 22, 2003 |
| FEI number | 3001452571 |
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