ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR — Class II medical device recall Z-1210-2018
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-1210-2018 |
|---|---|
| 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 | 165,750 |
| Reason classes | foreign material |
| Lot numbers | B00DHLP, L002FNL, L002V94 |
| Expiration dates | 2018-08, 2020-07, 2022-01 |
Product
ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR
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-1210-2018. 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.