Allied Vision Group Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact recall — FDA Z-1821-2020
Potentially counterfeit products in/and counterfeit packaging were imported to the U.S.
Overview of recall records associated with Allied Vision Group Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Potentially counterfeit products in/and counterfeit packaging were imported to the U.S.
This page summarizes recall records in which the official source identifies Allied Vision Group Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.