Class II — CooperVision Inc.
| Recalling firm | COOPERVISION, INC. |
|---|---|
| Registered facility | View this company's 14 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Incorrect power of lenses than the expected |
| Product | Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophilic) Contact Lens (extended wear) |
| Quantity | 24 |
| Distribution | US Nationwide Distribution |
| Initiated | 2020-01-13 |
| Classified | 2020-02-13 |
| Terminated | 2020-07-22 |
| Recall number | Z-1228-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — CooperVision Inc. (Z-1228-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/84725/
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