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Precision1 one-day contact lenses

Official notice

7 Oct 2025

Last checked

7 Oct 2025

Medium riskHealth Canada

An official Health Canada notice concerns Precision1 one-day contact lenses. Alcon is initiating a medical device recall for lot A8041128 of its Precision1™ Daily Soft Contact Lenses. We have identified the potential for a weak seal in some units within this specific lot. Our testing has confirmed the units are sealed; however, there is insufficient data to determine how the seal integrity may perform over the entirety of the labeled shelf life. As a result, Alcon is recalling lot A8041128 of its Precision1™ Daily Soft Contact Lenses. This event was identified internally. To date Alcon has not received any reports of complaints or adverse events related to this issue. Published 2025-10-07.

What to do now

Contact the manufacturer if you require additional information.

Recall number

78232

Official notice

2025-10-07

The hazard

Alcon is initiating a medical device recall for lot A8041128 of its Precision1™ Daily Soft Contact Lenses. We have identified the potential for a weak seal in some units within this specific lot. Our testing has confirmed the units are sealed; however, there is insufficient data to determine how the seal integrity may perform over the entirety of the labeled shelf life. As a result, Alcon is recalling lot A8041128 of its Precision1™ Daily Soft Contact Lenses. This event was identified internally. To date Alcon has not received any reports of complaints or adverse events related to this issue.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Lots

A8041128

Recall Numbers

78232

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Affected products

Product 1

Affected products - Precision1 One-Day Contact Lenses, Lot or serial number - A8041128, Model or catalogue number - 30003675-02.25D

Risk / hazard

Alcon is initiating a medical device recall for lot A8041128 of its Precision1™ Daily Soft Contact Lenses. We have identified the potential for a weak seal in some units within this specific lot. Our testing has confirmed the units are sealed; however, there is insufficient data to determine how the seal integrity may perform over the entirety of the labeled shelf life. As a result, Alcon is recalling lot A8041128 of its Precision1™ Daily Soft Contact Lenses. This event was identified internally. To date Alcon has not received any reports of complaints or adverse events related to this issue.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Alcon Laboratories, Precision1 One-day Contact Lenses.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

78232

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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