Class II — Johnson & Johnson Vision Care, Inc.
| Recalling firm | Johnson & Johnson Vision Care, Inc. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential that a limited number of individual contact lens packages have an incomplete packaging seal. |
| Product | ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50 |
| Quantity | 6,780 lenses |
| Distribution | Worldwide Distribution. US nationwide, Canada, Germany, Austria, Belgium, France, Luxemburg, Netherland, Portugal, Spain, Sweden, Switzerland, and Trinidad and Tobago. |
| Initiated | 2021-05-06 |
| Classified | 2021-06-16 |
| Terminated | 2021-11-02 |
| Recall number | Z-1865-2021 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Johnson & Johnson Vision Care, Inc. (Z-1865-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/87947/
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