Drug recall
EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for daily wear - Product Usage: indicated for the…
FDA recall event 87421 · Class II · Clerio Vision
Key facts
| Event ID | 87421 |
|---|---|
| Recall numbers | Z-1352-2021 |
| Recalling firm | Clerio Vision |
| Product type | Devices |
| Products | EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for daily wear - Product Usage: indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Contact lenses may be mislabeled with the incorrect lens power. |
| Initiation date | Feb 16, 2021 |
| Report date | Apr 14, 2021 |
| Termination date | Jul 5, 2023 |
| City | Sarasota |
| State | FL |
| Country | United States |
| FEI number | 3005184723 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: