Device recall
Z-0703-03: Glitter Eyes (tefilcon), daily wear soft (hydrophilic) contact lenses packed as…
FDA device recall · Class II · Ciba Vision Corporation
Key facts
| Recall number (Z-number) | Z-0703-03 |
|---|---|
| Recall event | 25796 |
| Product | Glitter Eyes (tefilcon), daily wear soft (hydrophilic) contact lenses packed as single units or kits in mulitple glass vials. |
| Product code | LPL |
| Recalling firm | Ciba Vision Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 7, 2004 |
| 510(k) numbers | K003071 |
| FEI number | 1053053 |
At a glance
- 1–9 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