{
  "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 I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "70818",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-0976-2015",
      "product_description": "0.9% Sodium Chloride Injection, USP, 250 mL,  Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.",
      "product_quantity": "9,912 VisIV flex containers",
      "reason_for_recall": "Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.",
      "recall_initiation_date": "20150305",
      "center_classification_date": "20150504",
      "termination_date": "20160609",
      "report_date": "20150513",
      "code_info": "Lot # 45-110-C6; Exp 03/1/16"
    }
  ]
}