{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Cincinnati",
      "address_1": "12011 Mosteller Rd",
      "reason_for_recall": "Due to FDA's safety communication relating to nontuberculous mycobacteria (NTM) infections related to heater/cooler devices, an updated Instructions For Use includes a more robust cleaning & disinfection procedure.",
      "address_2": "",
      "product_quantity": "1355 units",
      "code_info": "none",
      "center_classification_date": "20180215",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "OH",
      "product_description": "Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR  Product Usage:  A dual reservoir, water re-circulating device that supplies temperature controlled water to a heat exchanger. The device, in conjunction with a heat exchanger, is used to warm or cool the blood that enters and exits a blood heat exchanger for adult, pediatric or infant patients.",
      "report_date": "20180221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cincinnati Sub-Zero Products LLC",
      "recall_number": "Z-0629-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78173",
      "termination_date": "20180702",
      "more_code_info": "",
      "recall_initiation_date": "20171127",
      "postal_code": "45241-1528",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}