Alcon Air Optix Night & Day Aqua — Class II medical device recall Z-0609-2020
Completed recall by Lens.com, reported 2019-12-11. The product may be counterfeit and could have microbial issues.
| Recall number | Z-0609-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lens.com, Las Vegas, NV, United States |
| Recall initiated | 2018-08-14 |
| Classified | 2019-12-05 |
| Reported by FDA | 2019-12-11 |
| Reason classes | microbial contamination |
| Lot numbers | 2020/09, 2021/03, 2021/04, 2021/05, 2021/06, 2021/07, 2021/08, 2021/09, 31202568, 31231184, 31240720, 31242179, 31243321, 31247324, 31247744, 31248224, 31251559, 31251806, 31252252, 31252524, 31255298, 31256939, 31257909, 31257917, 31259174 |
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
The product may be counterfeit and could have microbial issues.
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-0609-2020. 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.