{
  "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": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76062",
      "recalling_firm": "Covidien LLC",
      "address_1": "60 Middletown Ave",
      "address_2": "N/A",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide.  Foreign:  Belgium  Germany  France  Netherlands",
      "recall_number": "Z-1125-2017",
      "product_description": "Covidien Nellcor SpO2 Forehead Sensor  Item Code: RS10;    The Covidien Nellcor¿ Forehead SpO2Sensor, model RS10, is indicated for use when continuous non-invasive arterial oxygen saturation and pulse rate monitoring are required for patients weighing more than 40 kg.",
      "product_quantity": "7453 Units",
      "reason_for_recall": "Labeling error: The label indicates the product is latex free, but the headband component included with the forehead sensor does contain latex.",
      "recall_initiation_date": "20161216",
      "center_classification_date": "20170202",
      "termination_date": "20181204",
      "report_date": "20170208",
      "code_info": "Lot Numbers:  161510095H, 161620089H, 161690203H, 161760132H, 161900091H,161970090H, 162040107H, 162110103H,  162320191H, 162390212H",
      "more_code_info": ""
    }
  ]
}