Device recall
Z-0766-2019: BW Lasso 2515 ANV eco Variable Diagnostic EP Catheter, REF D134301 Diagnostic…
FDA device recall · Class II · Stryker Sustainability Solutions
Key facts
| Recall number (Z-number) | Z-0766-2019 |
|---|---|
| Recall event | 81880 |
| Product | BW Lasso 2515 ANV eco Variable Diagnostic EP Catheter, REF D134301 Diagnostic electrophysiology (EP) catheters are specially designed electrode catheters that transmit electrical impulses and can be positioned for endocardial recording or stimulation. |
| Product code | NLH |
| Recalling firm | Stryker Sustainability Solutions |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 8, 2023 |
| 510(k) numbers | K112292 |
| FEI number | 3009350690 |
At a glance
- 1–9 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