{
  "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": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78327",
      "recalling_firm": "3M Company - Health Care Business",
      "address_1": "3m Center 2510 Conway Ave , B# 275-5-W-6",
      "address_2": "N/A",
      "postal_code": "55144-0001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA, MI, IL, MO, MN, GA, and Canada, Switzerland",
      "recall_number": "Z-0114-2018",
      "product_description": "3M Bair Hugger(TM) Normothermia System, Temperature Monitoring System Sensors Model 360 (Part Number 36000)",
      "product_quantity": "153 cases (3825 sensors)",
      "reason_for_recall": "During a recent investigation, 3M confirmed that a programming translation error could occur in a small amount of the sensors that could lead to a temperature readout that is lower than the patient\u0019s actual temperature.",
      "recall_initiation_date": "20171017",
      "center_classification_date": "20171118",
      "termination_date": "20201103",
      "report_date": "20171129",
      "code_info": "Lot Numbers:  17230, Exp. 2020 Aug 18; 17233, Exp. 2020 Aug 21; 17234, Exp. 2020 Aug 22; 17241, Exp. 2020 Aug 29"
    }
  ]
}