{
  "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": "62621",
      "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": "Nationwide distribution",
      "recall_number": "Z-2072-2012",
      "product_description": "EOS X-ray Medical Diagnostic , X-ray Equipment System    Digital Radiography used in general radiographic examination.",
      "product_quantity": "12 EOS Systems installed in the US",
      "reason_for_recall": "It was discovered of several generator failures of the EOS System due to failure of its anode controller board that drives the rotation of the X-ray tube anode.",
      "recall_initiation_date": "20120619",
      "center_classification_date": "20120928",
      "termination_date": "20130916",
      "report_date": "20121010",
      "code_info": "All associated Serial Numbers"
    }
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}