Device recall
Z-0846-06: Glaucoma Aqueous Shunt 365 mm, valved, P/N EG365V
FDA device recall · Class II · Eagle Vision Inc
Key facts
| Recall number (Z-number) | Z-0846-06 |
|---|---|
| Recall event | 35214 |
| Product | Glaucoma Aqueous Shunt 365 mm, valved, P/N EG365V |
| Product code | KYF |
| Recalling firm | Eagle Vision Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 13, 2006 |
| 510(k) numbers | K905703 |
| FEI number | 1000022662 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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