Device recall
Z-1863-2021: GENOSYL DS; Nitric Oxide Delivery System Combination Product NDA202860
FDA device recall · Class I · Vero Biotech, LLC
Key facts
| Recall number (Z-number) | Z-1863-2021 |
|---|---|
| Recall event | 87764 |
| Product | GENOSYL DS; Nitric Oxide Delivery System Combination Product NDA202860 |
| Product code | MRN |
| Recalling firm | Vero Biotech, LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Oct 12, 2023 |
| FEI number | 3014617112 |
At a glance
- None 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