FDA Device recall 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
- FDA Device
- Class II
- completed
- Published 2020-05-06
On 2020-05-06 the FDA classified a Class II recall of Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile by Allied Vision Group, citing potentially counterfeit products in/and counterfeit packaging were imported to the U.S.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1821-2020 |
| Classification | Class II |
| Status | completed |
| Initiated | 2018-08-01 |
| Published | 2020-05-06 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Allied Vision Group |
| Distribution | US |
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.
Identifiers
| code_info | Lot numbers 31202568; 31255298; 31257909; 31229117; 31252252. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1821-2020%22
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