{
  "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": {
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    {
      "status": "Terminated",
      "city": "LAKE FOREST",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82048",
      "recalling_firm": "ICU Medical Inc",
      "address_1": "600 N FIELD DRIVE",
      "address_2": "",
      "postal_code": "60045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0509-2019",
      "product_description": "0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only,  Hospira, Inc., Lake Forest, IL 60045 USA,  NDC 0409-7983-09",
      "product_quantity": "475320 bags",
      "reason_for_recall": "CGMP Deviations",
      "recall_initiation_date": "20190204",
      "center_classification_date": "20190219",
      "termination_date": "20200604",
      "report_date": "20190227",
      "code_info": "Lot #: 91-016-JT, Exp. July 01, 2020",
      "more_code_info": ""
    }
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}