FDA Device recall Z-1211-2018
1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
- FDA Device
- Class II
- terminated
- Published 2018-04-04
On 2018-04-04 the FDA classified a Class II recall of 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses by Johnson And Johnson Vision Care, citing some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1211-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-10-19 |
| Published | 2018-04-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Johnson And Johnson Vision Care |
| Distribution | US |
Product
1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
Reason
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Identifiers
| code_info | Lot B00LF41 Exp. 04/2021 Base Curve 8.5 Refractive Power -7.50D -1.25/180 Manufactured at J&J Vision Care Inc. Jacksonville, FL |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1211-2018%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.