Device recall
Z-1706-2010: AIR OPTIX (lotrafilcon B) for Astigmatism Soft Contact Lenses. CIBA Vision…
FDA device recall · Class II · Ciba Vision Corporation
Key facts
| Recall number (Z-number) | Z-1706-2010 |
|---|---|
| Recall event | 55570 |
| Product | AIR OPTIX (lotrafilcon B) for Astigmatism Soft Contact Lenses. CIBA Vision, Corp. Duluth, GA 30097. Toric lenses approved for daily wear and extended wear up to 6 nights. |
| Product code | LPM |
| Recalling firm | Ciba Vision Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 22, 2010 |
| PMA numbers | P010019, P010019S011 |
| FEI number | 1053053 |
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