{
  "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": "73832",
      "recalling_firm": "Neusoft Medical Systems Co., Ltd.",
      "address_1": "NO. 16 Shiji Road",
      "address_2": "Hunnan Industrial Area",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution - Including Puerto Rico and the states of IL, CT, SC, NE",
      "recall_number": "Z-1650-2016",
      "product_description": "NeuViz 64 Multi-Slice CT Scanner System (consist if two variants: NeuViz 64e, NeuViz 64i)",
      "product_quantity": "7 units",
      "reason_for_recall": "It was found by R&D in April, 2014 that there was a defect in NeuViz 64 system software version 1.0.5+P09.  The icons of side decubitus didn't meet the patient position description, when the scanner position was set to \"Right\" in the system setting - scanner options.",
      "recall_initiation_date": "20150502",
      "center_classification_date": "20160511",
      "termination_date": "20161104",
      "report_date": "20160518",
      "code_info": "Serial Numbers: N64E120022E, N64E130039E, N64I130051E, N64E130062E, N64E130063E, N64E130066E, N64I140077E"
    }
  ]
}