{
  "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": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "70174",
      "recalling_firm": "Hospira Inc.",
      "address_1": "375 N Field Dr",
      "address_2": "N/A",
      "postal_code": "60045-2513",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0334-2015",
      "product_description": "0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL  60045, NDC 0409-7984-11",
      "product_quantity": "30840 bags",
      "reason_for_recall": "Lack of Assurance of Sterility: The product has the potential for solution to leak at the administrative port.",
      "recall_initiation_date": "20141222",
      "center_classification_date": "20150107",
      "termination_date": "20150702",
      "report_date": "20150114",
      "code_info": "Lot #: 42-306-C6",
      "more_code_info": ""
    }
  ]
}