Device recall
Z-2323-2015: ReSTOR intraocular lens and ReSTOR Toric intraocular lens. The Alcon AcrySof IQ…
FDA device recall · Class I · Alcon Research, Ltd.
Key facts
| Recall number (Z-number) | Z-2323-2015 |
|---|---|
| Recall event | 71630 |
| Product | ReSTOR intraocular lens and ReSTOR Toric intraocular lens. The Alcon AcrySof IQ ReSTOR and IQ ReSTOR Toric intraocular lenses are posterior chamber lenses intended as optical implants designed to replace the human crystalline lens in adult patients following cataract surgery. The lenses subject to… |
| Product code | HQL |
| Recalling firm | Alcon Research, Ltd. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 30, 2017 |
| FEI number | 1610287 |
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