{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Jacksonville",
      "address_1": "7500 Centurion Pkwy",
      "reason_for_recall": "Limited number of individual contact lens packages may not have been completely sealed.",
      "address_2": "",
      "product_quantity": "36,330 lenses",
      "code_info": "Lot Numbers:   2054890422, +2.25D  2054890521, + 2.25D  2054895620, + 2.25D  1536500620, -3.75D  2138800422, -4.75D",
      "center_classification_date": "20130516",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) including states of: AL, AR, AZ, CA, CO, CT, DC, FL, GA, IL, IN, KY, LA, MA, MD, MI, MO, NC, NJ, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, WI and Puerto Rico; and countries of: Austria, Belgium, Canada, Costa Rica, Denmark, France, Germany, Hungary, India, Ireland, Israel, Italy, Korea, Japan, Luxembourg, Netherlands, Portugal, Norway, South Africa, Slovenia, Spain, Sweden, and United Kingdom.",
      "state": "FL",
      "product_description": "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.",
      "report_date": "20130522",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Johnson & Johnson Vision Care, Inc.",
      "recall_number": "Z-1335-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64468",
      "termination_date": "20130705",
      "more_code_info": "",
      "recall_initiation_date": "20121221",
      "postal_code": "32256-0517",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}