Coopervision Vertex Toric /2 Clear Toric- Power -2 — Class II medical device recall Z-1227-2020
Terminated recall by CooperVision Inc., reported 2020-02-19, distributed nationwide. Incorrect power of lenses than the expected
| Recall number | Z-1227-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperVision Inc., West Henrietta, NY, United States |
| Recall initiated | 2020-01-13 |
| Classified | 2020-02-13 |
| Reported by FDA | 2020-02-19 |
| Terminated | 2020-07-22 |
| Distributed | Nationwide (US) |
| Quantity | 216 units |
| Lot numbers | 15627000009010, 15627050004010, 16656000008010 |
Product
Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (extended wear)
Reason for recall
Incorrect power of lenses than the expected
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-1227-2020. 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.