{
  "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": "Broken Arrow",
      "state": "OK",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "72854",
      "recalling_firm": "Freedom Pharmaceuticals Inc",
      "address_1": "801 W New Orleans St",
      "address_2": "N/A",
      "postal_code": "74011-1844",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0573-2016",
      "product_description": "Baclofen USP powder, packaged in  (a)  25gm (4 oz container), (b) 100gm (16 oz container), (c) 500 gm (70 oz container), and (d) 1000 gm (120 oz container, Rx only, 801 W New Orleans St. Broken Arrow, OK 74011. NDC: (a) 52372-0909-25; (b) 52372-0909-01; (c) 52372-0909-50; (d) 52372-0909-10.",
      "product_quantity": "(a) 6 containers, (b) 42 containers, (c) 31 containers, (d) 253 containers",
      "reason_for_recall": "Presence of Foreign Substance",
      "recall_initiation_date": "20151109",
      "center_classification_date": "20160119",
      "termination_date": "20161223",
      "report_date": "20160127",
      "code_info": "Lot #: F10918, F10918-2, Exp: 07/24/2016; F10867, F10867A, Exp date: 03/11/2016",
      "more_code_info": ""
    }
  ]
}