← FDA ENFORCEMENT
Z-0326-2026Class II

Alcon Research LLC

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Alcon Research LLC
Product type
Device
Status
Ongoing
Report date
2025-11-05
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.
Firm state
TX
Product quantity
82 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Potential for a weak seal in some units resulting in compromise in sterility.

Product description

Alcon PRECISION1 One-Day Contact Lenses, -2.25D.

Code / lot info

GTIN: 00730822254946; Lot Number: A8041128

Other recalls SPEQ maps to Environmental Monitoring
See all Environmental Monitoring recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →