Device recall
Z-0740-04: FreshLook ColorBlends, Daily wear soft (hydrophilic) contact lens, BC: Median…
FDA device recall · Class III · Ciba Vision Corporation
Key facts
| Recall number (Z-number) | Z-0740-04 |
|---|---|
| Recall event | 28542 |
| Product | FreshLook ColorBlends, Daily wear soft (hydrophilic) contact lens, BC: Median, DIA: 14.5, Rx Only, Sterile, SPH -5.25, LOT ***, 2006-08, CIBA VISION Corporation, A Novartis Company, Duluth, GA 30007, USA, Made in USA. Product is packed in 6 packs. |
| Product code | LPM |
| Recalling firm | Ciba Vision Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 16, 2005 |
| 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