Official recall record

Precision1 One-Day Contact Lenses

What the authority reported

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

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

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