{
  "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": "2026-04-08",
    "results": {
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  },
  "results": [
    {
      "country": "United States",
      "city": "Louisville",
      "address_1": "826 Coal Creek Cir",
      "reason_for_recall": "Product was incorrectly assembled which could affect navigation accuracy of the device.",
      "address_2": "",
      "product_quantity": "1 unit",
      "code_info": "Product Number: 9736061  UDI (GTIN/UPN): 00763000123185  Serial Number: 000012585",
      "center_classification_date": "20200410",
      "distribution_pattern": "U.S.:  NY    No O.U.S.",
      "state": "CO",
      "product_description": "NavLock Tracker *** Rx Only",
      "report_date": "20200422",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Navigation, Inc.",
      "recall_number": "Z-1693-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "85318",
      "termination_date": "20210505",
      "more_code_info": "",
      "recall_initiation_date": "20190828",
      "postal_code": "80027-9710",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}