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 | Ongoing |
| Reason | The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power. |
| Product | Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90 |
| Quantity | 3150 |
| Distribution | Worldwide - US Nationwide distribution in the states of FL, IL, NY, UT, and WI. The country of Canada. |
| Initiated | 2023-02-14 |
| Classified | 2023-03-23 |
| Recall number | Z-1282-2023 |
| 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-1282-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91793/
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