{
  "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": "Louisville",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68145",
      "recalling_firm": "Medtronic Navigation, Inc.",
      "address_1": "826 Coal Creek Cir",
      "address_2": "N/A",
      "postal_code": "80027-9710",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-1586-2014",
      "product_description": "INSTRUMENT TRACKER 9733533XOM ENT 1PK",
      "product_quantity": "26,674 total",
      "reason_for_recall": "Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.",
      "recall_initiation_date": "20140424",
      "center_classification_date": "20141120",
      "termination_date": "20141229",
      "report_date": "20141126",
      "code_info": "Lot No.:  130904C  131203A  131003  131024B  130815  130904C  130510  130815  130708B  130815  130815  130716D  130204C  130418B  121128C  121218B  121218A  121128D  130409C  130409D  130123"
    }
  ]
}