{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70732",
      "recalling_firm": "Eos Imaging Inc",
      "address_1": "185 Alewife Brook Pkwy Ste 410",
      "address_2": "N/A",
      "postal_code": "02138-1104",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of: CA, DE, PA, MN, FL, MO, OH, IN and IL.",
      "recall_number": "Z-1460-2015",
      "product_description": "EOS, Digital radiography system used in general radiographic examinations.",
      "product_quantity": "13 units installed in US",
      "reason_for_recall": "When performing calibration, an alert message on the spectral filtration of the X-ray beam may be suppressed.  Improper filtration of the X-ray Beam can then occur in exams set up with copper filtration.",
      "recall_initiation_date": "20150217",
      "center_classification_date": "20150505",
      "termination_date": "20170531",
      "report_date": "20150513",
      "code_info": "Model Number - EOS System"
    }
  ]
}