Fort Lauderdale, FL, United States
Allied Vision Group Inc recalls
1 recall recorded since 2018, most recently on 1 August 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Completed Class II Medical devices
- Recall started
- 1 August 2018
- Reason
- Potentially counterfeit products in/and counterfeit packaging were imported to the U.S.
- Distribution
- Worldwide and US Nationwide
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1821-2020
- 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.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.