{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Greenville",
      "state": "SC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80896",
      "recalling_firm": "Hitachi Healthcare Americas Corp Informatics Division",
      "address_1": "204 Westfield St",
      "address_2": "N/A",
      "postal_code": "29601-1833",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "SC, CO, IL, AZ, MT, OH, IN, TX, GA, MA",
      "recall_number": "Z-2992-2018",
      "product_description": "VidiStar(TM) PACS & DICOM Viewer Software system",
      "product_quantity": "12 units",
      "reason_for_recall": "The secure filesystem client software used in the interface between the Vidistar PACS and an EHR system may cause intermixed images from multiple patients showing in a single study.",
      "recall_initiation_date": "20180828",
      "center_classification_date": "20180906",
      "termination_date": "20210211",
      "report_date": "20180912",
      "code_info": "versions 3.10.5 and 3.10.6"
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}