CLARITI 1 DAY TORIC Power -07 — Class II medical device recall Z-2152-2021
Terminated recall by CooperVision Inc., reported 2021-08-04, distributed nationwide. Misaligned placement of an axis mark can cause the patient to experience blurred vision
| Recall number | Z-2152-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperVision Inc., West Henrietta, NY, United States |
| Recall initiated | 2021-05-19 |
| Classified | 2021-07-27 |
| Reported by FDA | 2021-08-04 |
| Terminated | 2023-03-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, BR, CA, FR, NZ, TW |
| Quantity | 450 lenses |
| Lot numbers | W0106186 |
Product
CLARITI 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
Reason for recall
Misaligned placement of an axis mark can cause the patient to experience blurred vision
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-2152-2021. 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.