Device recall
Z-1568-2011: Polycarbonate prescription single vision lenses for use in sport goggles. To be…
FDA device recall · Class II · Luxottica Optical Manufacturing
Key facts
| Recall number (Z-number) | Z-1568-2011 |
|---|---|
| Recall event | 56120 |
| Product | Polycarbonate prescription single vision lenses for use in sport goggles. To be worn by a customer in a sport goggle frame to provide corrective refraction in accordance with the customer's prescription. Per the customer's request, some of the devices may also provide protection from bright… |
| Product code | HQG |
| Recalling firm | Luxottica Optical Manufacturing |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 19, 2012 |
| FEI number | 3008153912 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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