{
  "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": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75053",
      "recalling_firm": "Teleflex Medical",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "N/A",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) to CA and countries of:  Austria, Belgium, France, Germany, Italy, Japan, Poland, and Turkey.",
      "recall_number": "Z-0044-2017",
      "product_description": "Willy Rusch GmbH Tracheostomy Tube Set    Cannulation of tracheotomised patients, particularly in the case of a narrow tracheostoma and narrow-lumen tracheas. When using cannulas with curr. For short term intermittent inflation.",
      "product_quantity": "1095 units",
      "reason_for_recall": "The connector may disconnect from the tracheostomy tube during use.",
      "recall_initiation_date": "20160826",
      "center_classification_date": "20161018",
      "termination_date": "20170321",
      "report_date": "20161026",
      "code_info": "Lot - 15451, 15291, 15331, 15371, 15501, 15261, 15391, 15421, 15461, 15491"
    }
  ]
}