FDA Device recall Z-1744-2020
ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses
- FDA Device
- Class II
- terminated
- Published 2020-04-29
On 2020-04-29 the FDA classified a Class II recall of ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses by Johnson And Johnson Vision Care, citing package integrity failure observed during routine shift package integrity testing at an external re-packager.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1744-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-12-18 |
| Published | 2020-04-29 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Johnson And Johnson Vision Care |
| Distribution | US |
Product
ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90.
Reason
Package integrity failure observed during routine shift package integrity testing at an external re-packager.
Identifiers
| code_info | Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1744-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.