Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alcon Air Optix Night & Day Aqua (lotrafilcon A) Recalled by Lens.com Due to The product may be counterfeit and could have...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lens.com directly.
Affected Products
Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.
Quantity: 1,600/6-contact lens cartons
Why Was This Recalled?
The product may be counterfeit and could have microbial issues.
Where Was This Sold?
Due to HIPAA, the firm only provided a spreadsheet that contained the first name, last initial, and zip code of each customer who received email notification of the recall. Out of the 23,444 unique names on this list (25,162 names were actually listed due to multiple consumer orders), the firm believes approximately 800 of them to have received potentially counterfeit product. The recalling firm was requested to provide a consumer spreadsheet showing the name, shipping address, and email address but declined because they thought it would be a violation of HIPAA regulations.
About Lens.com
Lens.com has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report