{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Louisville",
      "address_1": "826 Coal Creek Cir",
      "reason_for_recall": "Medtronic Navigation, Inc. announces a voluntary field action for the AxIEM Touch N Go Pointer Probe because the patient registration accuracy may compromise navigation accuracy when using the StealthStation¿ System with Touch N Go Pointer Probes for patient registration.",
      "address_2": "",
      "product_quantity": "111 devices",
      "code_info": "lot number 150626B",
      "center_classification_date": "20170111",
      "distribution_pattern": "US Nationwide Distribution.",
      "state": "CO",
      "product_description": "AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed in a 30mil PETG tray sealed with a Tyvek lid and then placed in a shelf carton.",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Navigation, Inc.",
      "recall_number": "Z-1007-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76060",
      "termination_date": "20170519",
      "more_code_info": "",
      "recall_initiation_date": "20161212",
      "postal_code": "80027-9710",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}