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Precision1 One-Day Contact Lenses — recall 78232

Health Canada — Medical Devices · Canada · 2025-10-07 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 78232
Date of alert: 2025-10-07
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Ophthalmology
Product type: Medical devices

Reported risk: 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.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/precision1-one-day-contact-len

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Precision1 One-Day Contact Lenses — recall 78232

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