FDA Device recall Z-1335-2013
1-DAY ACUVUE MOIST Brand Contact Lenses, 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 1-DAY ACUVUE MOIST Brand Contact Lenses, 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-1335-2013 |
| 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
1-DAY ACUVUE MOIST Brand Contact Lenses, soft disposable contact lenses. The Vistakon (etafilcon A) Soft (hydrophilic) Contact Lens, Clear and Tinted (Visibility and/or Cosmetically), with UV Blocker for Daily Disposable Wear (spherical) is indicated for daily wear to enhance or alter the apparent color of the eye and/or for the correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with not diseased eyes who may have 1.00D or less of astigmatism.
Reason
Limited number of individual contact lens packages may not have been completely sealed.
Identifiers
| code_info | Lot Numbers: 2054890422, +2.25D 2054890521, + 2.25D 2054895620, + 2.25D 1536500620, -3.75D 2138800422, -4.75D |
|---|
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-1335-2013%22
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