Device recall
Z-0679-2025: Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part…
FDA device recall · Class II · Noah Medical
Key facts
| Recall number (Z-number) | Z-0679-2025 |
|---|---|
| Recall event | 95574 |
| Product | Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the Noah Medical Galaxy System (GAL-001) |
| 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