{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Fort Lauderdale",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84839",
      "recalling_firm": "Allied Vision Group Inc",
      "address_1": "5350 Nw 35th Ave",
      "address_2": "N/A",
      "postal_code": "33309-6314",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide and US Nationwide",
      "recall_number": "Z-1821-2020",
      "product_description": "Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.",
      "product_quantity": "655 boxes with 6 units per box.  total 3930",
      "reason_for_recall": "Potentially counterfeit products in/and counterfeit packaging were imported to the U.S.",
      "recall_initiation_date": "20180801",
      "center_classification_date": "20200429",
      "report_date": "20200506",
      "code_info": "Lot numbers 31202568; 31255298; 31257909; 31229117; 31252252."
    }
  ]
}