{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72583",
      "recalling_firm": "CareFusion 303, Inc.",
      "address_1": "10020 Pacific Mesa Blvd",
      "address_2": "N/A",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-US (nationwide) and the countries of Canada, Australia, and New Zealand.",
      "recall_number": "Z-0445-2016",
      "product_description": "Alaris Pump SmartSite Infusion Set, Model No. 2420-0500.    Used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein.",
      "product_quantity": "1,445,180 units",
      "reason_for_recall": "CareFusion is recalling the Alaris Pump Module SmartSite Infusion Set because the disconnection and leakage may occur during infusion.",
      "recall_initiation_date": "20151105",
      "center_classification_date": "20151223",
      "termination_date": "20170301",
      "report_date": "20151230",
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    }
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}