{
  "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": "New York",
      "state": "NY",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "70089",
      "recalling_firm": "Bethel Nutritional Consulting, Inc",
      "address_1": "599 W 190th St Ste 1",
      "address_2": "N/A",
      "postal_code": "10040-3577",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1207-2015",
      "product_description": "SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.",
      "product_quantity": "UNKNOWN",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling and analysis.",
      "recall_initiation_date": "20141219",
      "center_classification_date": "20150706",
      "termination_date": "20180627",
      "report_date": "20150715",
      "code_info": "Lot # 140430; Exp.12/17"
    }
  ]
}