Soft Contact Lens — Class II medical device recall Z-0529-2015
Terminated recall by Cooper Vision Caribbean Corp., reported 2014-12-17, distributed nationwide. Portions of the lots may contain units with an incorrect lens axis condition.
| Recall number | Z-0529-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cooper Vision Caribbean Corp., Juana Diaz, PR, United States |
| Recall initiated | 2014-10-28 |
| Classified | 2014-12-09 |
| Reported by FDA | 2014-12-17 |
| Terminated | 2015-10-02 |
| Distributed | Nationwide (US) |
| Quantity | 1,170 |
| Lot numbers | 8246525202, 8255525096 |
Product
Soft Contact Lens
Reason for recall
Portions of the lots may contain units with an incorrect lens axis condition.
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-0529-2015. 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.