Allied Vision Group Inc: Medical Device Recall in 2020 - (Recall #: Z-1821-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: August 1, 2018

Date Posted: May 6, 2020

Recall Number: Z-1821-2020

Event ID: 84839

Reason for Recall:

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

Status: Completed

Product Quantity: 655 boxes with 6 units per box. total 3930

Code Information:

Lot numbers 31202568; 31255298; 31257909; 31229117; 31252252.

Distribution Pattern:

Worldwide and US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated