{
  "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": "Research Triangle Park",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76263",
      "recalling_firm": "Teleflex Medical",
      "address_1": "2917 Weck Dr",
      "address_2": "",
      "postal_code": "27709-0186",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the state of  AZ, CA, CO, CT, FL, GA, IL, IN, KY, LA, MD, MA, MI, MN, MS, MO, NV, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, WI, and the countries of Canada and Mexico.",
      "recall_number": "Z-1519-2017",
      "product_description": "Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132    Product Usage:  To provide a patent airway for a patient with a blockage or potential blockage of the nasal cavity or nasopharynx.",
      "product_quantity": "7,600 eaches",
      "reason_for_recall": "Labeling error",
      "recall_initiation_date": "20170113",
      "center_classification_date": "20170321",
      "termination_date": "20250210",
      "report_date": "20170329",
      "code_info": "Lot/Batch Numbers 16A14 and 16A14",
      "more_code_info": ""
    }
  ]
}