Device recall
Z-0978-03: SOFT CONTACT LENSES (toric) packaged under the following labels: (1) CV \ ENCORE…
FDA device recall · Class III · Coopervision Inc
Key facts
| Recall number (Z-number) | Z-0978-03 |
|---|---|
| Recall event | 26532 |
| Product | SOFT CONTACT LENSES (toric) packaged under the following labels: (1) CV \ ENCORE toric (methafilcon A) and (2) ONEVUE 55 toric (methafilcon A) flexible wear. Responsible firm on label: Coopervision, Hamble, SO31, 4RF, UK, Scottsville, NY 14546, USA *** Made in UK. The lenses are sold in boxes of 6… |
| Product code | LPL |
| Recalling firm | Coopervision Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 11, 2005 |
| 510(k) numbers | K973063 |
| FEI number | 1314956 |
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