Precision1 One-Day Contact Lenses
Brand(s)
Last updated
Summary
Product
Precision1 One-Day Contact Lenses
Issue
Medical devices - Labelling and packaging
Medical devices - Sterility
What to do
Contact the manufacturer if you require additional information.
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Precision1 One-Day Contact Lenses | A8041128 | 30003675-02.25D |
Issue
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.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Ophthalmology
Companies
| Alcon Laboratories Inc. |
| 6201 South Freeway, Fort Worth, Texas, United States, 76134-2099 |
Published by
Health Canada
Audience
General public
Healthcare
Recall class
Type II
Recall date
Identification number
RA-78232
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