Device recall
Z-0095-06: CeeOn EDGE Silicone Posterior Chamber IOLs (Modelsl 911A and 913A)
FDA device recall · Class II · Advanced Medical Optics, Inc.
Key facts
| Recall number (Z-number) | Z-0095-06 |
|---|---|
| Recall event | 33849 |
| Product | CeeOn EDGE Silicone Posterior Chamber IOLs (Modelsl 911A and 913A) |
| Product code | HQL |
| Recalling firm | Advanced Medical Optics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2008 |
| PMA numbers | P990080 |
| FEI number | 3003843509 |
At a glance
- None 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