ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses — Class II medical device recall Z-1744-2020
Terminated recall by Johnson & Johnson Vision Care, Inc., reported 2020-04-29, distributed nationwide. Package integrity failure observed during routine shift package integrity testing at an external re-packager.
| Recall number | Z-1744-2020 |
|---|---|
| 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 | 2017-12-18 |
| Classified | 2020-04-17 |
| Reported by FDA | 2020-04-29 |
| Terminated | 2020-06-10 |
| Distributed | Nationwide (US) |
| Quantity | 150 lenses |
| Reason classes | packaging |
| Lot numbers | B00NKM0G |
Product
ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90.
Reason for recall
Package integrity failure observed during routine shift package integrity testing at an external re-packager.
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-1744-2020. 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.