{
  "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": "62571",
      "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": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA, including the states of AL, CO, FL, IA, MI, IA, NC, NE, NY and the countries of South Africa, Italy, and Spain.",
      "recall_number": "Z-2244-2012",
      "product_description": "Medtronic O-arm¿  Imaging System. Product Numbers: BI-700-00027-100, BI-700-00027-100R, BI-700-00027-120, BI-700-00027-120R, BI-700-00027-230, BI-700-00027-230R.",
      "product_quantity": "17 units",
      "reason_for_recall": "A fault in a high voltage relay in the 0-arm¿ Imaging System might cause the relay to overheat and burn.",
      "recall_initiation_date": "20120711",
      "center_classification_date": "20120822",
      "termination_date": "20160606",
      "report_date": "20120829",
      "code_info": "Serial Numbers: 109R, 118R, 124, 136, 159 ,170, 218,  222,  223, 236, 239 , 299, 309R,  402, 410, 412, 414."
    }
  ]
}