Device recall
Z-0342-03: Blue-Vis, CIBASOFT VISITINT, daily wear contact lens. Lot 1170119, Expiration…
FDA device recall · Class II · Ciba Vision Corporation
Key facts
| Recall number (Z-number) | Z-0342-03 |
|---|---|
| Recall event | 25101 |
| Product | Blue-Vis, CIBASOFT VISITINT, daily wear contact lens. Lot 1170119, Expiration 2007/10, BC 8.9, DIA 13.8, SPH -1.50, CIBA Vision, Corp, Duluth, GA 30097, Made in USA. |
| Product code | LPL |
| Recalling firm | Ciba Vision Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 28, 2003 |
| PMA numbers | P820086 |
| 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