FDA Device recall Z-1210-2018
ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR
- FDA Device
- Class II
- terminated
- Published 2018-04-04
On 2018-04-04 the FDA classified a Class II recall of ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR 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-1210-2018 |
| 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
ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR
Reason
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Identifiers
| code_info | Lot B00DHLP Exp. 08/2018 Base Curve 8.7, Refractive Power -10.00D - Manufactured in J&J Vision Care Inc. Jacksonville,…Lot B00DHLP Exp. 08/2018 Base Curve 8.7, Refractive Power -10.00D - Manufactured in J&J Vision Care Inc. Jacksonville, FL Lot L002FNL Exp. 07/2020 Base Curve 8.7 Refractive Power -4.75D Manufactured in J&J Vision Care Ireland Lot L002V94 Exp. 01/2022 Base Curve 8.7 Refractive Power -5.00D |
|---|
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-1210-2018%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.