Medical Device Recall: Z-0326-2026

FDA Recalls dataset · Firm: Alcon Research LLC · Status: Open, Classified

Recall Action Class: N/A Date Initiated: 2025-09-30 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0326-2026.

Recall Res Number
Z-0326-2026
Recalling Firm / Manufacturer
FEI Number
1610287
Recall Status
Open, Classified
Recall Classification
N/A
Date Initiated
2025-09-30
Date Posted
2025-10-24
Date Terminated
N/A
Product Code
LPL
Event Number
97739
Product Quantity
82 units
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.

Action Details Alcon notified consignees via letter on about 09/30/2025. Consignees were instructed to cease distribution of affected units to patients, review inventory to determine if affected units are on hand, dispose of all affected units, complete and return the response form, and forward the notification to other facilities or departments if product has been further distributed or transferred. For MARLO direct-to-patient shipments: As a part of our MARLO service, Alcon can notify patients who have received shipments directly from Alcon and initiate replacement on your behalf via the MARLO portal and app. You will receive a notification to opt in to this service in your ECP MARLO portal within the next week.

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.

Code Information / Serial Numbers GTIN: 00730822254946; Lot Number: A8041128

Related Establishments / Registrations

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