Alcon PRECISION1 One-Day Contact Lenses — Class II medical device recall Z-0326-2026
Ongoing recall by Alcon Research LLC, reported 2025-11-05, distributed in AL, AR, AZ, CT, FL, IA, ID, LA…. Potential for a weak seal in some units resulting in compromise in sterility.
| Recall number | Z-0326-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Alcon Research LLC, Fort Worth, TX, United States |
| Recall initiated | 2025-09-30 |
| Classified | 2025-10-24 |
| Reported by FDA | 2025-11-05 |
| Distributed | AL, AR, AZ, CT, FL, IA, ID, LA, MA, MD, MI, MN, NJ, NY, OK, OR, TN, TX, WA |
| Countries outside the US | CA |
| Quantity | 82 units |
| Reason classes | sterility, packaging |
| UPC / GTIN / UDI-DI | 00730822254946 |
| Lot numbers | A8041128 |
Product
Alcon PRECISION1 One-Day Contact Lenses, -2.25D.
Reason for recall
Potential for a weak seal in some units resulting in compromise in sterility.
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-0326-2026. 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.