{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Boulder",
      "address_1": "6135 Gunbarrel Ave",
      "reason_for_recall": "Covidien is recalling certain cuffed Shiley tracheostomy tubes due to consumer complaints related to the connections and functions of the inner and outer cannula which were observed during mechanical ventilation of patients.",
      "address_2": "",
      "product_quantity": "337,227 units",
      "code_info": "United States distributed product includes:  8FEN lots 0910000342 to 1101001558 and 110300622X to 120600700X; 8LPC lots 0910000348 to 1101001823 and 110200327X to 120600351X.    Product Distributed outside of the United States:  8FENJ lots 1003002176, 1004000412, and 120100433X.  8FEN-S lot 0910001010; 8FENJ-S lots 0910002075 to 1103002299 and 110601803X to 120402125X; and 8LPC-S lots 0910001002 to 1103002052 and 111000400X to 120600014X.",
      "center_classification_date": "20120810",
      "distribution_pattern": "Worldwide Distribution - US Nationwide",
      "state": "CO",
      "product_description": "Shiley Reusable Cannula Low Pressure Cuffed Tracheostomy Tubes, model numbers (Worldwide) 8LPC, 8FEN; (Outside U.S.) 8FENJ, 8FENJ-S, 8LPC-S, 8FEN-S.      Product Usage:  The product is intended for use to bypass upper airway obstructions, provide long term ventilation, support and/or manage tracheal/bronchial secretions.  The product is sold as sterile.  The packaging may indicate either Covidien or Tyco as the manufacturer as the firm has transitioned from Tyco to Covidien over the past 4 years.",
      "report_date": "20120822",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Nellcor Puritan Bennett Inc. (dba Covidien LP)",
      "recall_number": "Z-2174-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62559",
      "termination_date": "20150122",
      "more_code_info": "",
      "recall_initiation_date": "20120718",
      "postal_code": "80301-3214",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}