{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "LAKE FOREST",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "80213",
      "recalling_firm": "ICU Medical Inc",
      "address_1": "600 N FIELD DRIVE",
      "address_2": "N/A",
      "postal_code": "60045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Canada",
      "recall_number": "D-0883-2018",
      "product_description": "0.9% Sodium Chloride Injection, USP, 100 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7984-23",
      "product_quantity": "525984 bags",
      "reason_for_recall": "Lack of assurance of sterility: Bags have potential to leak.",
      "recall_initiation_date": "20180531",
      "center_classification_date": "20180620",
      "termination_date": "20200604",
      "report_date": "20180627",
      "code_info": "Lot #: 85-016-JT, Exp 01/01/2020"
    }
  ]
}