Device recall
Z-0125-2010: ClearSight(TM) 1-Day (ocufilcon D) Toric 30 daily disposable contact lenses for…
FDA device recall · Class III · CooperVision Inc.
Key facts
| Recall number (Z-number) | Z-0125-2010 |
|---|---|
| Recall event | 53532 |
| Product | ClearSight(TM) 1-Day (ocufilcon D) Toric 30 daily disposable contact lenses for astigmatism --- Name and Address on Label: CooperVision Hamble, SO31 4RF, UK, and Scottsville, NY 14546 USA --- Each lens is supplied sterile in a blister containing buffered saline solution. The blister is labeled with… |
| Product code | MVN |
| Recalling firm | CooperVision Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 12, 2012 |
| FEI number | 3005724763 |
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