Device recall
Z-0598-2026: Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number…
FDA device recall · Class II · Noah Medical Corporation
Key facts
| Recall number (Z-number) | Z-0598-2026 |
|---|---|
| Recall event | 97656 |
| Product | Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Description: The Galaxy SystemTM and its accessories are intended to provide bronchoscopic visualization of and access to patient airways for diagnostic and therapeutic procedure. |
| Product code | EOQ |
| Recalling firm | Noah Medical Corporation |
| 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