Alcon PRECISION1 One-Day Contact Lenses Recalled for Weak Seal and Sterility Risk

Agency Publication Date: October 24, 2025

Summary

Alcon Research LLC has recalled 82 units of Alcon PRECISION1 One-Day Contact Lenses (-2.25D) because some units may have a weak seal on the packaging. This defect could compromise the sterility of the lenses, making them unsafe to use. The affected lenses were distributed in several U.S. states and Canada and are identified by Lot Number A8041128. If you have these lenses, stop using them immediately and contact your eye care provider or the manufacturer.

Risk

A weak seal in the packaging can allow bacteria or other microorganisms to contaminate the lens. Using non-sterile contact lenses poses a risk of eye infections, which could lead to serious inflammation or vision damage.

What You Should Do

This recall affects Alcon PRECISION1 One-Day Contact Lenses (-2.25D) packaged with GTIN 00730822254946 and Lot Number A8041128.
Stop using the product. Return it to the place of purchase for a refund or replacement, throw it away, or contact your healthcare provider or Alcon Research LLC for further instructions.
Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

Option 1: Full Refund

How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement

Option 2: Dispose of Product

How to: Stop using and throw the product away.

Affected Products

Product: Alcon PRECISION1 One-Day Contact Lenses (-2.25D)

Variants: -2.25D, One-Day

Lot Numbers:

A8041128

GTIN:

00730822254946

Recall #: Z-0326-2026

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 97739

Status: Active

Manufacturer: Alcon Research LLC

Sold By: Authorized eye care providers

Manufactured In: United States

Units Affected: 82 units

Distributed To: Alabama, Arizona, Arkansas, Connecticut, Florida, Idaho, Iowa, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, New Jersey, New York, Oklahoma, Oregon, Tennessee, Texas, Washington

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.