{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Corpus Christi",
      "state": "TX",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "73973",
      "recalling_firm": "Making It a Lifestyle",
      "address_1": "6202 Beechwood Dr",
      "address_2": "N/A",
      "postal_code": "78412-4744",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0221-2017",
      "product_description": "BLACK GOLD X ADVANCED capsules, 60-count bottles, Manufactured for: Making it A Lifestyle, L.L.C.",
      "product_quantity": "1000 bottles",
      "reason_for_recall": "Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.",
      "recall_initiation_date": "20160429",
      "center_classification_date": "20161222",
      "termination_date": "20200930",
      "report_date": "20161228",
      "code_info": "All Lots"
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}