Device recall
Z-2801-2011: iSymm Intraocular Lens (Model FC-60AD) The Hoya iSymm Model FC-60AD Intraocular…
FDA device recall · Class II · Hoya Surgical Optics, Inc.
Key facts
| Recall number (Z-number) | Z-2801-2011 |
|---|---|
| Recall event | 59207 |
| Product | iSymm Intraocular Lens (Model FC-60AD) The Hoya iSymm Model FC-60AD Intraocular Lens (IOL) is an ultraviolet-light absorbing posterior chamber intraocular lens designed to be implanted posterior to the iris where the lens will replace the optical function of the natural crystalline lens. However… |
| Product code | HQL |
| Recalling firm | Hoya Surgical Optics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 29, 2012 |
| FEI number | 3006723646 |
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