Device recall
Z-0135-2027: JenaValve Trilogy Delivery Catheter, Size 25MM REF: TRILOGY-DC-M
FDA device recall · Class II · Jenavalve Technology Inc.
Key facts
| Recall number (Z-number) | Z-0135-2027 |
|---|---|
| Recall event | 99697 |
| Product | JenaValve Trilogy Delivery Catheter, Size 25MM REF: TRILOGY-DC-M |
| Product code | NPT |
| Recalling firm | Jenavalve Technology Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P250024 |
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