ACUVUE VITA soft — Class II medical device recall Z-1865-2021
Terminated recall by Johnson & Johnson Vision Care, Inc., reported 2021-06-23, distributed nationwide. Potential that a limited number of individual contact lens packages have an incomplete packaging seal.
| Recall number | Z-1865-2021 |
|---|---|
| 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 | 2021-05-06 |
| Classified | 2021-06-16 |
| Reported by FDA | 2021-06-23 |
| Terminated | 2021-11-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, CA, CH, DE, ES, FR, PT, SE, TT |
| Quantity | 6,780 lenses |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00733905989612 |
Product
ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50
Reason for recall
Potential that a limited number of individual contact lens packages 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-1865-2021. 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.