{
  "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": "Little Rock",
      "state": "AR",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "72028",
      "recalling_firm": "Cantrell Drug Company",
      "address_1": "7321 Cantrell Rd",
      "address_2": "N/A",
      "postal_code": "72207-4144",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1152-2016",
      "product_description": "fentaNYL citrate in 0.9% Sodium Chloride Injection, 10 mcg/1 mL (10 mcg/mL), in 1 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-024-45, UPC: 0100352533024450",
      "product_quantity": "884 syringes",
      "reason_for_recall": "Subpotent Drug",
      "recall_initiation_date": "20150821",
      "center_classification_date": "20160706",
      "termination_date": "20170203",
      "report_date": "20160713",
      "code_info": "Lot: 6234, exp 9/20/15"
    }
  ]
}