{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "77357",
      "recalling_firm": "Global Marketing Enterprises, Inc.",
      "address_1": "1801 S Canal St",
      "address_2": "N/A",
      "postal_code": "60616-1522",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "KY, VA, MI",
      "recall_number": "D-1096-2017",
      "product_description": "Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g (8.8 oz)., 1250 servings, Packed By:  LifeLine Nutrients Corp, 1801 S. Canal St, Chicago, IL 60616, UPC 021754905076",
      "product_quantity": "52.5 kg",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA:  The product consists of pure, powdered caffeine and is an unapproved drug due to stimulant claims.  The product is also misbranded as it fails to bear adequate directions for its intended use.",
      "recall_initiation_date": "20170522",
      "center_classification_date": "20170817",
      "termination_date": "20220825",
      "report_date": "20170823",
      "code_info": "Batch # 15121931, 15121939, Exp 12/19"
    }
  ]
}