24K Premium Lense — Class II medical device recall Z-2270-2024
Ongoing recall by Ontact Inc, reported 2024-07-17, distributed nationwide. Contact lenses recalled due to potential bacterial contamination.
| Recall number | Z-2270-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ontact Inc, Riverside, CA, United States |
| Recall initiated | 2024-03-20 |
| Classified | 2024-07-05 |
| Reported by FDA | 2024-07-17 |
| Distributed | Nationwide (US) |
| Quantity | 2,842 |
| Reason classes | microbial contamination |
Product
24K Premium Lense, Distributed by Updream Inc.
Reason for recall
Contact lenses recalled due to potential bacterial contamination.
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-2270-2024. 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.