{
  "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": "Stamford",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75192",
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "address_1": "419 West Ave",
      "address_2": "N/A",
      "postal_code": "06902-6343",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution.",
      "recall_number": "Z-0073-2017",
      "product_description": "Fujifilm Synapse PACS, Software versions: 4.0.xxx,  4.1.xxx, version 4.2.xxx, version 4.3.xxx    Medical imaging and information management system, SYNAPSE allows the archiving and distribution of image information from all modalities",
      "product_quantity": "251 units",
      "reason_for_recall": "Image data for a patient\u0019s image may not be correct",
      "recall_initiation_date": "20160915",
      "center_classification_date": "20161012",
      "termination_date": "20190220",
      "report_date": "20161019",
      "code_info": "Software versions: 4.0.xxx,  4.1.xxx, version 4.2.xxx, version 4.3.xxx"
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}