{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Minneapolis",
      "address_1": "6000 Nathan Ln N",
      "reason_for_recall": "Packaged with an incorrect size inner cannula.",
      "address_2": "",
      "product_quantity": "7,840",
      "code_info": "Item code/product number: 100/856/080  lot number: 3578884",
      "center_classification_date": "20190604",
      "distribution_pattern": "Worldwide Distribution - US Nationwide AL, CA, CT, FL, IL, KY, MA, MD, NC, NJ, OH, OR, PA, RI, SC, TN, UT, and VA.  Canada, UK and Ireland",
      "state": "MN",
      "product_description": "Portex Blue Line Ultra Tracheostomy Tube Inner Cannula.  One cannula comes inside a package which is labeled in part,     Product Usage:  The Portex Blue Line Ultra¿ Tracheostomy Tubes are indicated for airway maintenance of tracheostomized patients.",
      "report_date": "20190612",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Smiths Medical ASD Inc.",
      "recall_number": "Z-1732-2019",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "82387",
      "termination_date": "20201102",
      "more_code_info": "",
      "recall_initiation_date": "20190211",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}