{
  "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": "69494",
      "recalling_firm": "Hospira Inc.",
      "address_1": "275 N Field Dr",
      "address_2": "N/A",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide, Puerto Rico, and U.S. Virgin Islands.",
      "recall_number": "D-0282-2015",
      "product_description": "5% Dextrose and 0.9% Sodium Chloride Injection, USP, 1000 mL container,  Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045,  NDC 0409-7941-09.",
      "product_quantity": "340,272 bags",
      "reason_for_recall": "Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.",
      "recall_initiation_date": "20141014",
      "center_classification_date": "20141125",
      "termination_date": "20151228",
      "report_date": "20141203",
      "code_info": "Lot # 32-104-JT; Exp. 08/15  Lot # 34-136-JT; Exp. 10/15  Lot # 36-092-JT; Exp. 12/15",
      "more_code_info": ""
    }
  ]
}