{
  "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": [
    {
      "status": "Terminated",
      "city": "Miami",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69386",
      "recalling_firm": "Dharma Research, Inc.",
      "address_1": "5220 Nw 72nd Ave",
      "address_2": "Bay 15",
      "postal_code": "33166-4860",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US Distribution in states of: CA, PA, FL, IL, including Puerto Rico; and countries of: Honduras, Dominican Republic, Turkey, Nicaragua, Colombia, Pakistan, Trinidad & Tobago, Guatemala, Phillipines, Saudi Arabia, and United Arab Emirates.",
      "recall_number": "Z-0475-2015",
      "product_description": "Dharma Cavity Varnish with Fluoride",
      "product_quantity": "2,842",
      "reason_for_recall": "During an FDA inspection, it was found that the products are being marketed without a cleared 510k.",
      "recall_initiation_date": "20140929",
      "center_classification_date": "20141126",
      "termination_date": "20161003",
      "report_date": "20141203",
      "code_info": "All Lots - Item #14-00015",
      "more_code_info": ""
    }
  ]
}