{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Vernon Hills",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81021",
      "recalling_firm": "Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company",
      "address_1": "330 Corporate Woods Pkwy",
      "address_2": "",
      "postal_code": "60061-3107",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: US (nationwide) to states of: AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, including PR; and countries of: Austria, Canada, Czech Republic, Chile, Cyprus, Ecuador, Estonia, Germany, Greece, Italy, Japan, and Switzerland.",
      "recall_number": "Z-0720-2019",
      "product_description": "Portex  Unit Dose 15 ml Normal Saline    ¿",
      "product_quantity": "357,552",
      "reason_for_recall": "Lack of sterility assurance:  leaking containers which could lead to exposure to infectious agents.",
      "recall_initiation_date": "20170905",
      "center_classification_date": "20190204",
      "termination_date": "20240416",
      "report_date": "20190213",
      "code_info": "Model # R0159   Lot Numbers: ¿A661, B067, A526, A536, A569, and B201",
      "more_code_info": ""
    }
  ]
}