MyDay Toric — Class II medical device recall Z-1014-2023
Ongoing recall by CooperVision, Inc., reported 2023-02-01, distributed in CA, FL, IA, KY, NC, NY, OH, OR…. Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.
| Recall number | Z-1014-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperVision, Inc., West Henrietta, NY, United States |
| Recall initiated | 2022-12-27 |
| Classified | 2023-01-24 |
| Reported by FDA | 2023-02-01 |
| Distributed | CA, FL, IA, KY, NC, NY, OH, OR, WI |
| Countries outside the US | CA, JP |
| Quantity | 6,570 lenses |
| Lot numbers | 21514501939036, 21514501972036, 6474502034 |
Product
MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use.
Reason for recall
Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.
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-1014-2023. 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.