{
  "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": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80092",
      "recalling_firm": "Smiths Medical ASD Inc.",
      "address_1": "6000 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to CA, FL, GA, ID, NJ, NM, OH, VA.      International distribution to France.",
      "recall_number": "Z-2114-2018",
      "product_description": "Bivona¿ Tracheostomy Tube Tracheostomy Tubes",
      "product_quantity": "16 units",
      "reason_for_recall": "Carton labeling is printed with \"Sterile\" indicated labeling, however the device is not sold as sterile.",
      "recall_initiation_date": "20180402",
      "center_classification_date": "20180607",
      "termination_date": "20181114",
      "report_date": "20180613",
      "code_info": "Part No. (Lot No.): CMZ3241N (DS009716), ST16EN80NSC194N (DS009794),   SU15AN70NSC153N (DS009577), FT17IN60NGC114N (DS009894), CMZ3331N (DS009761), XU17GS50NSF046N (DS009609), FT17IN60NGC114N (DS009861), AA16ES70NSC110N (DS009586), FT17IN70NSC111N (DS009856),    FT16IN60NGC053N (DS009540), FU15AN55NSA076N (DS009464), AT17IS60NGC105N (DS009811)"
    }
  ]
}