{
  "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": "65894",
      "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, Puerto Rico, and internet sales",
      "recall_number": "D-371-2014",
      "product_description": "Quick Thin (citrus aurantium extract, sweet potato fiber, cyamopsis gum powder, alfalfa, mulberry leaf, guarana, spirulina) capsules, 400 mg, 30-count bottle, Distributed by: Bethel, Inc., Tel: (212) 568-5330.",
      "product_quantity": "9,121 bottles",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of sibutramine, N-Desmethylsibutramine and phenolphthalein. Sibutramine and phenolphthalein were previously available drug products but were removed from the U.S. market making these products unapproved new drugs.",
      "recall_initiation_date": "20130805",
      "center_classification_date": "20131218",
      "termination_date": "20180530",
      "report_date": "20131225",
      "code_info": "Lot 10032011, Exp 10/14"
    }
  ]
}