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 | Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil. |
| Product | ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR |
| Quantity | 165,750 |
| Distribution | Worldwide distribution. US nationwide including Puerto Rico, Korea, Czech Republic, China, Japan, Great Britain, Austria, Malaysia, Hong Kong, Russia, Taiwan, Singapore, India, and Brazil |
| Initiated | 2017-10-19 |
| Classified | 2018-03-27 |
| Terminated | 2020-06-12 |
| Recall number | Z-1210-2018 |
| 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-1210-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/79152/
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