{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Torrance",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81080",
      "recalling_firm": "Shimadzu Medical Systems Usa Com",
      "address_1": "20101 S Vermont Ave",
      "address_2": "N/A",
      "postal_code": "90502-1328",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic: LA",
      "recall_number": "Z-0197-2019",
      "product_description": "TRINIAS Digital Angiographic System intended to be used for cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body radiographic/fluoroscopic procedures.",
      "product_quantity": "1",
      "reason_for_recall": "Due to a software issue the C-arm may unexpectedly moved when being moved to the park position and during specific operations. There is a possibility the C-arm will come into contact with a patient or healthcare personnel.",
      "recall_initiation_date": "20180615",
      "center_classification_date": "20181019",
      "termination_date": "20210428",
      "report_date": "20181031",
      "code_info": "Model Trinias  UDI (01)04540217049080(11)170727(21)41E58C977001  Serial Number 41E58C977001"
    }
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}