Alcon Research LLC: Device Recall

Recall #Z-0326-2026 · 09/30/2025

Class II: Risk

Recall Details

Recall Number
Z-0326-2026
Classification
Class II
Product Type
Device
Recalling Firm
Alcon Research LLC
Status
Ongoing
Date Initiated
09/30/2025
Location
Fort Worth, TX, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
82 units

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.

Distribution Pattern

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.

Other Recalls by Alcon Research LLC

View all recalls by Alcon Research LLC →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.