1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses — Class II medical device recall Z-1211-2018
Terminated recall by Johnson & Johnson Vision Care, Inc., reported 2018-04-04, distributed nationwide. Some contact lenses were associated with complaints of a foreign matter caught between the blister package and
| Recall number | Z-1211-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Johnson & Johnson Vision Care, Inc., Jacksonville, FL, United States |
| Recall initiated | 2017-10-19 |
| Classified | 2018-03-27 |
| Reported by FDA | 2018-04-04 |
| Terminated | 2020-06-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BR, CN, CZ, GB, HK, IN, JP, KR, MY, RU, SG, TW |
| Quantity | 56,070 |
| Reason classes | foreign material |
| Lot numbers | B00LF41 |
| Expiration dates | 2021-04 |
Product
1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
Reason for recall
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
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-1211-2018. 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.