{
  "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": "77384",
      "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": "E-Mail",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-3036-2017",
      "product_description": "Samsung GU60A system-  Digital X-ray Imaging Systems are intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications",
      "product_quantity": "87 units",
      "reason_for_recall": "When performing the Stitching function on GU60A system, unintended area is exposed to radiation",
      "recall_initiation_date": "20170524",
      "center_classification_date": "20170825",
      "termination_date": "20180709",
      "report_date": "20170906",
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