{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Munich",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82304",
      "recalling_firm": "Brainlab AG",
      "address_1": "Olof-palme-str. 9",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution: US (Nationwide) and countries of:  Australia, Austria, Belgium, Canada, Czech Republic, Denmark, Ecuador, France, Germany, Greece, Hong Kong, Ireland, Italy, Japan, Kazakhstan, Malaysia, New Zealand, Philippines, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand and United Kingdom.",
      "recall_number": "Z-1082-2019",
      "product_description": "Spine & Trauma 3D Navigation 1.0 (subpart of the system  Navigation Software Spine & Trauma 3D, Version 3.0 )     Intended Use The Spine & Trauma Navigation System is intended as an intraoperative image-guided localization system to enable minimally invasive surgery.",
      "product_quantity": "148 units",
      "reason_for_recall": "In certain occurrences, the affected navigation software application might unexpectedly display a navigated instrument in an axial, coronal/sagittal (ACS) view representation with fixed planes in the image reconstruction (the  not-updated ACS view ), instead of displaying the desirable view representation  Inline View , which is commonly used for navigating invasive instruments at the spine. This could lead the surgeon to be unable to determine the position of the navigated instrument. This might occur after a  crash restore  or after changing between different navigation workflows during the same patient treatment.",
      "recall_initiation_date": "20190227",
      "center_classification_date": "20190415",
      "termination_date": "20190710",
      "report_date": "20190424",
      "code_info": "Version 1.0.0.249, GTIN 04056481140328"
    }
  ]
}