Device recall
Z-1673-2009: Optiflex Lens Positioning Unit (LPU) Product Code: 10970, for use in…
FDA device recall · Class II · Volk Optical Inc
Key facts
| Recall number (Z-number) | Z-1673-2009 |
|---|---|
| Recall event | 52461 |
| Product | Optiflex Lens Positioning Unit (LPU) Product Code: 10970, for use in vitreoretinal ophthalmic surgical procedures. |
| Product code | KYB |
| Recalling firm | Volk Optical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 12, 2012 |
| FEI number | 1000122772 |
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