Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Completed

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.

FDA Recall Z-1821-2020 · Posted None

Recalling FirmAllied Vision Group Inc
Recall StatusCompleted
Product CodeLPM
Date Initiated2018-08-01
Product Quantity655 boxes with 6 units per box. total 3930

Reason for Recall

Potentially counterfeit products in/and counterfeit packaging were imported to the U.S.

Firm Action

The firm initiated the recall by email on August 01, 2018 and followed with a second email on August 03, 2018. The email explained that the product was potentially non-genuine and offered a full refund or exchange of the product.

Root Cause

Counterfeit

Distribution Pattern

Worldwide and US Nationwide

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑