{
  "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": "Danvers",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78679",
      "recalling_firm": "NeuroLogica Corporation",
      "address_1": "14 Electronics Ave",
      "address_2": "N/A",
      "postal_code": "01923-1011",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide US",
      "recall_number": "Z-0726-2018",
      "product_description": "The GC80 Digital X-ray Imaging System",
      "product_quantity": "45 units",
      "reason_for_recall": "An image was obtained with over exposure during a Thorax examination using the AEC function.",
      "recall_initiation_date": "20170622",
      "center_classification_date": "20180302",
      "termination_date": "20181005",
      "report_date": "20180314",
      "code_info": "Accession Number 1310459"
    }
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}