{
  "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": "Label has the incorrect size for the tracheotomy tube.",
      "address_2": "",
      "product_quantity": "3 units",
      "code_info": "Lot# 3952216",
      "center_classification_date": "20200909",
      "distribution_pattern": "US Distribution to state of: CT",
      "state": "MN",
      "product_description": "Bivona Mid-Range Aire-Cuf Adult Tracheostomy Tube    This tube is intended to provide direct airway access for a tracheotomized patient for up to 29 days. It may be reprocessed up to 10 times for single patient use.",
      "report_date": "20200916",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Smiths Medical ASD Inc.",
      "recall_number": "Z-2946-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "86345",
      "termination_date": "20210513",
      "more_code_info": "",
      "recall_initiation_date": "20200828",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}