FDA Medical devices recall ·
Alcon PRECISION1 One-Day Contact Lenses, -2.25D recall
- Recall number
- Z-0326-2026
- Date
- (initiated September 30, 2025)
- Company / brand
- Alcon Research LLC
6201 South Fwy, Fort Worth, TX, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 82 units
- Hazard tags
- Sterility
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Alcon PRECISION1 One-Day Contact Lenses, -2.25D.
Why was it recalled?
Potential for a weak seal in some units resulting in compromise in sterility.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
GTIN: 00730822254946; Lot Number: A8041128
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.
States: Alabama Arkansas Arizona Connecticut Florida Iowa Idaho Louisiana Massachusetts Maryland Michigan Minnesota New Jersey New York Oklahoma Oregon Tennessee Texas Washington
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0326-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.