Device recall
Z-1561-2022: NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG), Part…
FDA device recall · Class I · Synapse Biomedical Inc
Key facts
| Recall number (Z-number) | Z-1561-2022 |
|---|---|
| Recall event | 90626 |
| Product | NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG), Part No. 23-0021. |
| Product code | OIR |
| Recalling firm | Synapse Biomedical Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Oct 24, 2023 |
| FEI number | 3005868392 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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