Total1 and Total30 Contact Lenses
Brand(s)
Summary
If affected, stop use and contact your eye care provider or retailer for guidance on next steps.
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Total30 (Lehfilcon A) Soft Contact Lenses | See manufacturer’s website | 30004013+02.50D 30004013-03.50D 30004013-04.75D 30004013-05.75D 30004013-02.75D 30004013-04.25D 30004013-05.25D 30004013-06.00D 30004013-1.50D 30004013-00.75D 30004013-02.50D 30004013+03.00D 30004013-01.25D 30004013-02.25D 30004013-03.25D 30004013-04.00D 30004013-04.50D 30004013-08.50D 30004013-01.00D 30004013-02.00D 30004013-05.00D |
| Soft Contact Lens delefilcon A Multifocal | See manufacturer’s website | 30003623+00.25D 30003625-01.25D 30003625-02.75D 30003623+01.75D 30003624-08.50D 30003625+01.75D 30003625+02.25D 30003625-05.50D 30003625-06.50D 30003623+03.75D 30003623+04.00D 30003623-06.00D 30003625+01.25D 30003625+02.00D 30003625-02.25D 30003625-04.00D 30003625-05.00D 30003625-08.00D 30003623+03.25D 30003623-03.00D 30003623-08.50D 30003625+01.50D 30003625+02.50D 30003625+03.00D 30003625-01.00D 30003625-02.00D 30003625-02.50D 30003623-01.25D 30003625-04.25D 30003623-05.00D 30003625-05.25D 30003623-00.50D 30003625-00.75D 30003625-03.75D 30003625-04.50D |
| Dailies Total1 One-Day Contact Lenses For Astigmatism | See manufacturer’s website | 900263595-00.75D 900263595-01.75D 30003964+01.75D 900263595+02.50D 900263595-02.75D 900263595-03.00D 900263595+00.75D 900263595+01.50D 900263595-00.50D 900263595-02.25D 900263595-05.00D 900263595-06.00D 900263595-06.50D 30003964-00.50D 900263595+01.00D 900263595-05.50D 30003964-00.25D 30003964-03.75D 900263595-03.50D 900263595-01.50D 900263595-04.25D 900263595-04.50D 900263595-04.75D 30003964-01.75D 30003964-03.00D 900263595+03.50D 900263595+04.00D 900263595-03.75D |
Issue
Alcon has initiated a Voluntary Medical Device Field Correction for specific lots of DAILIES TOTAL1® for Astigmatism, DAILIES TOTAL1® Multifocal and TOTAL30® Sphere contact lenses. An isolated quality issue was identified with a material supplied by a third-party vendor that was used in the production of contact lenses at a single manufacturing site. As a result, the affected lenses may not meet Alcon quality and/or performance standards for the entirety of their labeled shelf life.
The contact lenses from the identified lots are not expected to cause an increased risk to the wearer. As with any contact lens, there is a remote likelihood that wearing a lens from the affected lots may lead to temporary issues such as irritation, redness, or blurred vision. These symptoms typically resolve after lens removal and/or replacement (as directed in the patient leaflet1).
You can confirm if a lot number of contact lenses is within the scope of the medical device recall at https://www.myalcon.com/search-my-lot/. If you have an affected lot number, please discontinue use of the product and contact your eye care provider or the retailer where you purchased the contact lenses for further information on next steps.
Recall start date: August 13, 2024
Additional information
Details
| Alcon Laboratories Inc. |
| 6201 South Freeway, Fort Worth, Texas, United States, 76134-2099 |
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