# FDA recall Z-1821-2020

> **Allied Vision Group Inc** · Class II · device recall initiated 2018-08-01.

## 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 for recall

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

## Distribution

Worldwide and US Nationwide

## Key facts

- **Recall number:** Z-1821-2020
- **Recalling firm:** Allied Vision Group Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2018-08-01
- **Report date:** 2020-05-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fort Lauderdale, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1821-2020

## Citation

> AI Analytics. FDA recall Z-1821-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1821-2020. Source: US FDA. Licensed CC0.

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