Device recall
Z-0620-2016: Boston Scientific, MRI PROPONENT" SR, REF L210 Pacemaker. These devices treat…
FDA device recall · Boston Scientific Corporation
Key facts
| Recall number (Z-number) | Z-0620-2016 |
|---|---|
| Recall event | 72855 |
| Product | Boston Scientific, MRI PROPONENT" SR , REF L210 Pacemaker. These devices treat bradycardia (slow heartbeats) with RA and/or RV pacing therapy as necessary |
| Product code | LWP |
| Recalling firm | Boston Scientific Corporation |
| Status | Terminated |
| Termination date | Mar 8, 2016 |
| 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