Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1336-2013 — 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

U.S. FDA — Device Enforcement · United States · 2012-12-21 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1336-2013
Date of alert: 2012-12-21
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Johnson & Johnson Vision Care, Inc.
Product category: device
Product type: Devices

Reported risk: Limited number of individual contact lens packages may not have been completely sealed.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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