Device recall
Z-2280-2019: GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm).
FDA device recall · Class II · Codman & Shurtleff Inc
Key facts
| Recall number (Z-number) | Z-2280-2019 |
|---|---|
| Recall event | 83502 |
| Product | GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm). |
| Product code | HCG |
| Recalling firm | Codman & Shurtleff Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 4, 2020 |
| 510(k) numbers | K171862 |
| FEI number | 3013875781 |
At a glance
- 1–9 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