{
  "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": "Boulder",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71583",
      "recalling_firm": "Covidien LP (formerly Nellcor Puritan Bennett Inc.)",
      "address_1": "6135 Gunbarrel Ave",
      "address_2": "N/A",
      "postal_code": "80301-3214",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide including Canada.",
      "recall_number": "Z-2267-2015",
      "product_description": "OxiMax N-65 Handheld Pulse Oximeter.     N65, N65-1, N65P, and N65P-1.  For continuous or spot check monitoring of functional arterial oxygen saturation (SpO2) and pulse rate.",
      "product_quantity": "211,426 units",
      "reason_for_recall": "Potential missing segments on the display that can result in misinterpretation of data.",
      "recall_initiation_date": "20150629",
      "center_classification_date": "20150727",
      "termination_date": "20171103",
      "report_date": "20150805",
      "code_info": "All Lots of Product Code N650, N65, N65-1, N65P, N65P-1"
    }
  ]
}