{
  "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": [
    {
      "status": "Terminated",
      "city": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80747",
      "recalling_firm": "COVIDIEN LLC",
      "address_1": "15 Hampshire St",
      "address_2": "N/A",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states:  CA, CO, FL, GA, IA, IL, IN, KY, LA, MA, MD, MO, NC, NJ, NY, OH, OR, PA, RI, SC, TN, TX, VA, and WA.",
      "recall_number": "Z-3204-2018",
      "product_description": "TEMP SENSE SILICONE 14FR5CC2W, Item Code 50514T",
      "product_quantity": "27515 total",
      "reason_for_recall": "The temperature sensor catheters may be defective in that they will show a lower body temperature measurement than the actual temperature of the patient.",
      "recall_initiation_date": "20180711",
      "center_classification_date": "20180920",
      "termination_date": "20200803",
      "report_date": "20180926",
      "code_info": "1733850164  1805050064"
    }
  ]
}