Alcon Research LLC recalls Alcon PRECISION1 One-Day Contact Lenses
- Recalling company
- Alcon Research LLC
- Product
- Alcon PRECISION1 One-Day Contact Lenses, -2.25D.
- Reason
- Potential for a weak seal in some units resulting in compromise in sterility.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Sep 30, 2025
- Reported
- Nov 5, 2025
- Distribution
- Worldwide - US distribution in the states of Alabama, Arizona, Arkansas, Connecticut, Florida, Idaho, Iowa, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, New Jersey, New York, Oklahoma, Oregon, Tennessee, Texas, Washington and the country of Canada.
- Status
- Ongoing
- Quantity
- 82 units
- Lot / codes
- GTIN: 00730822254946; Lot Number: A8041128
- Company location
- Fort Worth, TX
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0326-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0326-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.