PRECISION1 Contact Lenses (Alcon) – sterility seal (2025)
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Alcon PRECISION1 One-Day Contact Lenses, -2.25D.
Brand
Alcon Research LLC
Lot Codes / Batch Numbers
GTIN: 00730822254946, Lot Number: A8041128
Products Sold
GTIN: 00730822254946; Lot Number: A8041128
Alcon Research LLC is recalling Alcon PRECISION1 One-Day Contact Lenses, -2.25D. due to Potential for a weak seal in some units resulting in compromise in sterility.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for a weak seal in some units resulting in compromise in sterility.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, AR, CT, FL, ID, IN, IA, LA, MD, MA, MI, MN, NJ, NY, OK, OR, TN, TX, WA
Page updated: Jan 10, 2026