{
  "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-1596-2014",
      "product_description": "SPHERES 8801075 5/TRAY 12PK",
      "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.:  1207251  1301091  1301081  1211141  1301151  1302051  1303141  1303121  1303191  1304031  1304081  1303071  1305221  1305281  1306181  1306231  1307041  1307051  1307111  1307131  1307121"
    }
  ]
}