Device recall
Z-0825-2025: ALTRUA 2 DR Pacemaker, SL (Model Number S702) and EL (Model Number S722)
FDA device recall · Class I · Boston Scientific Corporation
Key facts
| Recall number (Z-number) | Z-0825-2025 |
|---|---|
| Recall event | 95969 |
| Product | ALTRUA 2 DR Pacemaker, SL (Model Number S702) and EL (Model Number S722) |
| Product code | LWP |
| Recalling firm | Boston Scientific Corporation |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 2124215 |
At a glance
- None 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