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 | Package integrity failure observed during routine shift package integrity testing at an external re-packager. |
| Product | ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90. |
| Quantity | 150 lenses. |
| Distribution | Nationwide US. |
| Initiated | 2017-12-18 |
| Classified | 2020-04-17 |
| Terminated | 2020-06-10 |
| Recall number | Z-1744-2020 |
| 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-1744-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85261/
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