Recall Z-1821-2020— Allied Vision Group Inc

Name: FDA recall Z-1821-2020
Creator: U.S. Food and Drug Administration
Published: 2018-08-01

Class II · Completed

Class II FDA medical device recall by Allied Vision Group Inc, initiated 2018-08-01. FDA's recall record names no specific 510(k) clearance for this event. Product: 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.. Reason: Potentially counterfeit products in/and counterfeit packaging were imported to the U.S..

Recalling firm: Allied Vision Group Inc
Classification: Class II
Status: Completed
Initiated: 2018-08-01
Firm location: Fort Lauderdale, FL, United States

Product description

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.

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.