{
  "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": "Shenyang",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75383",
      "recalling_firm": "Neusoft Medical Systems Co., Ltd.",
      "address_1": "NO. 16 Shiji Road",
      "address_2": "Hunnan Industrial Area",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution",
      "recall_number": "Z-0875-2017",
      "product_description": "NeuViz 64  Multi-slice  CT Scanner Systems",
      "product_quantity": "23 units",
      "reason_for_recall": "The Firm discovered during contrast agent tracking scan, when the expected concentration of contrast agent is reached, later planned scan may be interrupted. The system must be powered down and restarted to clear the interruption error before scanning can resume.",
      "recall_initiation_date": "20160831",
      "center_classification_date": "20161223",
      "termination_date": "20180104",
      "report_date": "20170104",
      "code_info": "NeuViz 64e, NeuViz 64i with software version 1.0.6.3258 +P04 or previous version.    NeuViz 64En, NeuViz 641n with software version 1.0.7.4021+P05 or previous version"
    }
  ]
}