ACUVUE OASYS for ASTIGMATISM brand contact lenses — Class II medical device recall Z-1131-2019
Terminated recall by Johnson & Johnson Vision Care, Inc., reported 2019-04-17, distributed in CA. One lot of ACUVUE OASYS¿ for ASTIGMATISM Brand Contact lenses has the potential for a limited number of indivi
| Recall number | Z-1131-2019 |
|---|---|
| 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 | 2019-03-11 |
| Classified | 2019-04-11 |
| Reported by FDA | 2019-04-17 |
| Terminated | 2021-12-06 |
| Distributed | CA |
| Quantity | 300 lenses |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00733905669460 |
Product
ACUVUE OASYS for ASTIGMATISM brand contact lenses, Base Curve 8.6 Refractive Power -1.00D, -1.25D x 100, 6 pack.
Reason for recall
One lot of ACUVUE OASYS¿ for ASTIGMATISM Brand Contact lenses has the potential for a limited number of individual contact lens packages to have an incomplete packaging seal.
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-1131-2019. 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.