Device recall
Z-0564-2024: VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number…
FDA device recall · Class II · Vero Biotech, LLC
Key facts
| Recall number (Z-number) | Z-0564-2024 |
|---|---|
| Recall event | 93475 |
| Product | VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates and delivers nitric oxide (NO) for inhalation at the point of use |
| Product code | MRN |
| Recalling firm | Vero Biotech, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 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