Clariti 1-day toric soft contact lenses — Class II medical device recall Z-1282-2023
Ongoing recall by CooperVision, Inc., reported 2023-03-29, distributed nationwide. The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the inco
| Recall number | Z-1282-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperVision, Inc., West Henrietta, NY, United States |
| Recall initiated | 2023-02-14 |
| Classified | 2023-03-23 |
| Reported by FDA | 2023-03-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 3,150 |
| Lot numbers | W0124677 |
Product
Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90
Reason for recall
The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1282-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.