Alcon PRECISION1 One-Day Contact Lenses recall: Sterility Concern
Alcon PRECISION1 One-Day Contact Lenses, -2.25D.
Why was Alcon PRECISION1 One-Day Contact Lenses recalled?
Potential for a weak seal in some units resulting in compromise in sterility.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
GTIN: 00730822254946; Lot Number: A8041128
- Product
- Alcon PRECISION1 One-Day Contact Lenses, -2.25D.
- Recalling firm
- Alcon Research LLC
- Quantity
- 82 units
- 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.
- Recall date
- November 5, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)