Alcon Air Optix Night & Day Aqua — Class II medical device recall Z-1821-2020
Completed recall by Allied Vision Group Inc, reported 2020-05-06, distributed nationwide. Potentially counterfeit products in/and counterfeit packaging were imported to the U.S.
| Recall number | Z-1821-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Allied Vision Group Inc, Fort Lauderdale, FL, United States |
| Recall initiated | 2018-08-01 |
| Classified | 2020-04-29 |
| Reported by FDA | 2020-05-06 |
| Distributed | Nationwide (US) |
| Lot numbers | 31202568, 31229117, 31252252, 31255298, 31257909 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1821-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.