Device recall
Z-2405-2015: RenLane Renal Denervation Catheter; Cat No.: D135601. Used in adults patients…
FDA device recall · Class II · Cordis Corporation
Key facts
| Recall number (Z-number) | Z-2405-2015 |
|---|---|
| Recall event | 70741 |
| Product | RenLane Renal Denervation Catheter; Cat No.: D135601. Used in adults patients (>18 years) with drug resistant hypertension to denervate the renal arteries to reduce blood pressure. |
| Product code | MPB |
| Recalling firm | Cordis Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 26, 2015 |
| FEI number | 1016427 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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