Device recall
Z-1802-2010: Medtronic Racer Biliary Stent System, Model number XD518YF, UPC code…
FDA device recall · Class II · Medtronic CardioVascular
Key facts
| Recall number (Z-number) | Z-1802-2010 |
|---|---|
| Recall event | 53126 |
| Product | Medtronic Racer Biliary Stent System, Model number XD518YF, UPC code 00721902758164 in a box containing sterilized pouch with product, manufactured by Medtronic Vascular, Sunnyvale, CA. Medical device system consisting of a balloon-expandable intraluminal stent premounted onto the balloon of an over… |
| Product code | FGE |
| Recalling firm | Medtronic CardioVascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 31, 2011 |
| 510(k) numbers | K032768 |
| FEI number | 3001452571 |
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