{
  "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-0716-2019",
      "product_description": "Intermed 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿",
      "product_quantity": "16,104 Japan only",
      "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 # 0552IMJ Lot Numbers: ¿Z588 and  Z597",
      "more_code_info": ""
    }
  ]
}