Device recall
Z-0808-2021: Clerio Vision, extreme H2O monthly, MED, DIA 14.0 PWR -2.25, UPC 675506803334 (6…
FDA device recall · Class II · Clerio Vision
Key facts
| Recall number (Z-number) | Z-0808-2021 |
|---|---|
| Recall event | 86952 |
| Product | Clerio Vision, extreme H2O monthly, MED, DIA 14.0 PWR -2.25, UPC 675506803334 (6 count) and UPC 675506804478 (12 count) - Product Usage: for daily wear is indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or hyperopic. The lens may… |
| Product code | LPL |
| Recalling firm | Clerio Vision |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 5, 2023 |
| FEI number | 3005184723 |
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