Device recall
Z-0742-2025: Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of and…
FDA device recall · Class II · Noah Medical
Key facts
| Recall number (Z-number) | Z-0742-2025 |
|---|---|
| Recall event | 95585 |
| Product | Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of and access to patient airways for diagnostic and therapeutic procedures. |
| Product code | EOQ |
| Recalling firm | Noah Medical |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K223144 |
| FEI number | 3021325287 |
At a glance
- 1–9 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