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

FDA Recall #Z-0326-2026 — Class II — September 30, 2025

Recall #Z-0326-2026 Date: September 30, 2025 Classification: Class II Status: Ongoing

Product Description

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

Reason for Recall

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

Recalling Firm

Alcon Research LLC — Fort Worth, TX

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product 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.

Code Information

GTIN: 00730822254946; Lot Number: A8041128

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated