FDA Device recall Z-1336-2013
ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR, Soft, disposable contact lenses
- FDA Device
- Class II
- terminated
- Published 2013-05-22
On 2013-05-22 the FDA classified a Class II recall of ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR, Soft, disposable contact lenses by Johnson And Johnson Vision Care, citing limited number of individual contact lens packages may not have been completely sealed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1336-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-12-21 |
| Published | 2013-05-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Johnson And Johnson Vision Care |
| Distribution | US |
Product
ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR, Soft, disposable contact lenses. The Vistakon (galyfilcon A) Contact Lens is indicated for daily wear for the correction of refractive ametropia (myopia and hyperopia) in aphakic or non-aphakic persons with non-diseased eyes who may have 1.00D of astigmatism or less.
Reason
Limited number of individual contact lens packages may not have been completely sealed.
Identifiers
| code_info | Lot Codes: B00DJPQ, -7.00D B00DMHZ, -6.00D B00DMJP, +4.00D |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1336-2013%22
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