{
  "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": "Littleton",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "61741",
      "recalling_firm": "Medtronic Navigation, Inc.",
      "address_1": "300 Foster St",
      "address_2": "N/A",
      "postal_code": "01460-2017",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide Distribution including the states of CO,  IN, and MN.",
      "recall_number": "Z-1849-2012",
      "product_description": "Medtronic 0-arm Imaging System with Software Version 3.1.1, Catalog Numbers: BI-700-00027-120R and BI-700-00027-120. The 0-arm¿ Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging.",
      "product_quantity": "3 units",
      "reason_for_recall": "Software Version 3.1.1 does not meet navigational accuracy.",
      "recall_initiation_date": "20101012",
      "center_classification_date": "20120621",
      "termination_date": "20120621",
      "report_date": "20120627",
      "code_info": "Serial Numbers:  125, 156, 234R."
    }
  ]
}