{
  "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": "Punxsutawney",
      "state": "PA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "73167",
      "recalling_firm": "Bee Xtreme",
      "address_1": "506 N Penn St",
      "address_2": "N/A",
      "postal_code": "15767-1527",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Unknown",
      "recall_number": "D-0021-2017",
      "product_description": "Jenesis Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA",
      "product_quantity": "13 bottles",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein",
      "recall_initiation_date": "20151223",
      "center_classification_date": "20161012",
      "termination_date": "20170130",
      "report_date": "20161019",
      "code_info": "All Lots"
    }
  ]
}