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 Allied Vision Group Inc Due to Potentially counterfeit products in/and counterfeit packaging were imported...
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 Allied Vision Group Inc 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: 655 boxes with 6 units per box. total 3930
Why Was This Recalled?
Potentially counterfeit products in/and counterfeit packaging were imported to the U.S.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Allied Vision Group Inc
Allied Vision Group Inc 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