What's being recalled
Companies: Alcon Laboratories Inc., 6201 South Freeway, Fort Worth, Texas, United States, 76134-2099.
How to identify it
Affected products: Precision1 One-Day Contact Lenses; Lot or serial number: A8041128; Model or catalogue number: 30003675-02.25D
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.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)