{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Shenzhen",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95288",
      "recalling_firm": "FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO.,LTD",
      "address_1": "No. 1304 Science And Technology Innovation Park, Shajing Dahong",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "International distribution to the countries of China and Hong Kong.",
      "recall_number": "Z-3306-2024",
      "product_description": "DVOT SARS-CoV-2 ANTIGEN TEST KIT, Model Number FCY-AGT-01",
      "product_quantity": "150,000 kits",
      "reason_for_recall": "The \"DVOT brand\" rapid test kits have not obtained the necessary authorization to be sold in the United States.",
      "recall_initiation_date": "20240626",
      "center_classification_date": "20240927",
      "report_date": "20241009",
      "code_info": "All lots in the United States"
    }
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}