{
  "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": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70793",
      "recalling_firm": "Smiths Medical ASD, Inc.",
      "address_1": "1265 Grey Fox Rd",
      "address_2": "N/A",
      "postal_code": "55112-6929",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "MN",
      "recall_number": "Z-1692-2015",
      "product_description": "Smiths Medical, BCI Advisor Vital Signs Monitor, Product Reorder No 92M774325A.",
      "product_quantity": "5  UPDATE 4-20-2015 to include 10 additional devices",
      "reason_for_recall": "The Auxiliary Serial Input/ Output Modes on the Advisor do not function as expected, resulting in data formatting issues or  incorrect data being transmitted in or out of the serial port into a data collection system.",
      "recall_initiation_date": "20150321",
      "center_classification_date": "20150529",
      "termination_date": "20151120",
      "report_date": "20150610",
      "code_info": "Serial Numbers:  4059587 through 4059591    UPDATED 4-20-2015:  additional devices affected have serial numbers:  4059949, 4059950, 4059951, 4059952, 4059953, 4059954, 4059955, 4059957, 4059958 and 4059960"
    }
  ]
}