{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Peachtree Corners",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76279",
      "recalling_firm": "The See Clear Company",
      "address_1": "4995 Buford Hwy Ste 102",
      "address_2": "N/A",
      "postal_code": "30071-2721",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) including states of: AZ, CA, DE, FL, GA, HI, LA, NJ, NY, NV, ON, PA and WA; and  country of: Canada.",
      "recall_number": "Z-1404-2017",
      "product_description": "Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition, Circle Collection, Lunatic, Fright, Desire and See Clear.",
      "product_quantity": "119,829 units",
      "reason_for_recall": "Sterility and Misbranding: Lenses may not be sterile and may be labeled with erroneous lot numbers and expiry dates.",
      "recall_initiation_date": "20170106",
      "center_classification_date": "20170303",
      "report_date": "20170315",
      "code_info": "All lots of lenses sold between 10/31/2013 to 10/31/2016"
    }
  ]
}