{
  "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": "Terminated",
      "city": "Bronx",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Food",
      "event_id": "85882",
      "recalling_firm": "Sundial Herbal Products",
      "address_1": "3609 Boston Rd",
      "address_2": "N/A",
      "postal_code": "10466-5810",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NY",
      "recall_number": "F-1502-2020",
      "product_description": "\"SUNDIAL***ETHIOPIAN ABISH (FENNUGREEK SEED POWDER.)***\"",
      "product_quantity": "Unknown",
      "reason_for_recall": "Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.",
      "recall_initiation_date": "20200630",
      "center_classification_date": "20200915",
      "termination_date": "20221026",
      "report_date": "20200909",
      "code_info": "Product manufactured, processed, packed, held, and/or distributed during the time period beginning 1/1/2014 through 5/27/2020."
    }
  ]
}