{
  "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": "\"Manufactured\" and \"Use By\" labels are transposed incorrectly suggesting the product expires before it was manufactured.",
      "address_2": "",
      "product_quantity": "12,000 devices",
      "code_info": "Lot numbers 1703221A and 1705111A",
      "center_classification_date": "20181004",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of  AR, CA, GA, IN, LA, OK, MA, MI, NC, NJ, NV, SC, TX, VA, and  WV.  There was government distribution and no military distribution.  Foreign distribution was made to Poland and Russia.",
      "state": "MN",
      "product_description": "smiths medical portex First Breath Adult Nasal Cannula, REF 001283, Non-flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style.      Product Usage:  For the administration of nasal oxygen and humidity to patients.",
      "report_date": "20181010",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Smiths Medical ASD Inc.",
      "recall_number": "Z-0071-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80635",
      "termination_date": "20190430",
      "more_code_info": "",
      "recall_initiation_date": "20180706",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}