Device recall
Z-0096-06: CeeOn Heparin Surface Modified (HSM) PMMA One-Piebe Posterior Chambet- IOLs…
FDA device recall · Class II · Advanced Medical Optics, Inc.
Key facts
| Recall number (Z-number) | Z-0096-06 |
|---|---|
| Recall event | 33849 |
| Product | CeeOn Heparin Surface Modified (HSM) PMMA One-Piebe Posterior Chambet- IOLs (Models:722C, 722Y, 811C, 812C and 812CU) |
| Product code | HQL |
| Recalling firm | Advanced Medical Optics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2008 |
| PMA numbers | P960034 |
| 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