Drug recall
Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophilic) Contact Lens (extended…
FDA recall event 84725 · Class II · CooperVision Inc.
Key facts
| Event ID | 84725 |
|---|---|
| Recall numbers | Z-1227-2020, Z-1228-2020 |
| Recalling firm | CooperVision Inc. |
| Product type | Devices |
| Products | Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophilic) Contact Lens (extended wear), Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (extended wear) |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect power of lenses than the expected |
| Initiation date | Jan 13, 2020 |
| Report date | Feb 19, 2020 |
| Termination date | Jul 22, 2020 |
| City | West Henrietta |
| State | NY |
| Country | United States |
| FEI number | 3005724763 |
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: