1-DAY ACUVUE MOIST Brand Contact Lenses — Class II medical device recall Z-1335-2013
Terminated recall by Johnson & Johnson Vision Care, Inc., reported 2013-05-22, distributed nationwide. Limited number of individual contact lens packages may not have been completely sealed.
| Recall number | Z-1335-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Johnson & Johnson Vision Care, Inc., Jacksonville, FL, United States |
| Recall initiated | 2012-12-21 |
| Classified | 2013-05-16 |
| Reported by FDA | 2013-05-22 |
| Terminated | 2013-07-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, CA, CR, DE, DK, ES, FR, GB, HU, IE, IL, IN, IT, JP, KR, LU, NL, NO, PT, SE, SI, ZA |
| Quantity | 36,330 lenses |
| Lot numbers | 1536500620, 2.25D, 2054890422, 2054890521, 2054895620, 2138800422, 3.75D, 4.75D |
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 for recall
Limited number of individual contact lens packages may not have been completely sealed.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1335-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.