{
  "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": "67935",
      "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",
      "recall_number": "D-1261-2014",
      "product_description": "Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2  mEq/mL), 20 mL Single-dose Fliptop Vial, For IV use, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA",
      "product_quantity": "255,900 vials",
      "reason_for_recall": "Presence of Particulate; red and black particulate within the solution and embedded within the plastic vial identified as iron oxide",
      "recall_initiation_date": "20140327",
      "center_classification_date": "20140424",
      "termination_date": "20150630",
      "report_date": "20140430",
      "code_info": "Lot 22-127-DK",
      "more_code_info": ""
    }
  ]
}