{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Paris France",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66833",
      "recalling_firm": "EOS Imaging",
      "address_1": "10 rue Mercoeur 4 Ieme Etage",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-0529-2014",
      "product_description": "EOS System X- ray beam    Digital radiography system used in general radiographic examinations.",
      "product_quantity": "22 EOS systems are installed in US",
      "reason_for_recall": "EOS imaging discovered during production internal testing that the X-ray beam collimation set up by the operator at the user interface of the acquisition workstation is different from the actual collimation of  the X-ray beam operated by the EOS system during the X-ray acquisition.",
      "recall_initiation_date": "20131107",
      "center_classification_date": "20140109",
      "termination_date": "20150127",
      "report_date": "20140115",
      "code_info": "EOS System",
      "more_code_info": ""
    }
  ]
}