{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75557",
      "recalling_firm": "Smiths Medical ASD, Inc.",
      "address_1": "1265 Grey Fox Rd",
      "address_2": "N/A",
      "postal_code": "55112-6929",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Internationally to Finland",
      "recall_number": "Z-1145-2017",
      "product_description": "HOTLINE Blood and Fluid Warmer, Mole l HL-90.  Designed for use with the Hotline Fluid Warming Set (L-80, L-70 and L-70N) to warm blood and intravenous (I.V.) fluids and deliver them to the patient's intravenous access site at normothermic temperatures under gravity flow conditions.",
      "product_quantity": "33",
      "reason_for_recall": "HOTLINE Blood and Fluid Warmers included Greek and Danish language labeling instead of the required Finnish labeling.",
      "recall_initiation_date": "20161031",
      "center_classification_date": "20170207",
      "termination_date": "20171127",
      "report_date": "20170215",
      "code_info": "S101B06231-235; S101B06318-325/327; S101B06354-362; S101B06464-473."
    }
  ]
}