Device recall
Z-0271-2016: Expansion of previous recall of AcrySof IQ ReSTOR and AcrySof IQ ReSTOR Toric…
FDA device recall · Class I · Alcon Research, Ltd.
Key facts
| Recall number (Z-number) | Z-0271-2016 |
|---|---|
| Recall event | 72377 |
| Product | Expansion of previous recall of AcrySof IQ ReSTOR and AcrySof IQ ReSTOR Toric IOL; now to include AcrySof IQ Toric models SN6AT6, SN6AT7, SN6AT8, and SN6AT9. Intended for primary implantation in the capsular bag of the eye for visual correction. |
| 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