Device recall
Z-2480-2025: DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113…
FDA device recall · Class I · Medtronic Perfusion Systems
Key facts
| Recall number (Z-number) | Z-2480-2025 |
|---|---|
| Recall event | 97295 |
| Product | DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113 LV VENT 13FR, Model Number 12113 |
| Product code | DWF |
| Recalling firm | Medtronic Perfusion Systems |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K834039 |
| FEI number | 1000116158 |
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