{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Stamford",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67958",
      "recalling_firm": "Fujifilm Medical System USA, Inc.",
      "address_1": "419 West Ave",
      "address_2": "N/A",
      "postal_code": "06902-6343",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Distribution including the states of TX and KY and Internationally to China.",
      "recall_number": "Z-1642-2014",
      "product_description": "MXR-35 Diagnostic X-ray High Voltage Generator manufactured by DRGEM Corporation.    x-ray generator",
      "product_quantity": "14",
      "reason_for_recall": "The MXR-35 X-ray Generator's labeling did not include the certification statement as required by 21 CFR Part 10 10.2.",
      "recall_initiation_date": "20120629",
      "center_classification_date": "20140521",
      "termination_date": "20180601",
      "report_date": "20140528",
      "code_info": "SN:  MXA1170108, MXA1270262"
    }
  ]
}