{
  "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": "Rochester",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65369",
      "recalling_firm": "Carestream Health Inc.",
      "address_1": "150 Verona St",
      "address_2": "",
      "postal_code": "14608-1733",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) including the countries of Austria, Australia, Belgium, Canada, China, Finland, France, Germany, Italy, Korea, Kuwait, Saudi Arabia, Spain, Sweden, Switzerland, Taiwan, United Kingdom.",
      "recall_number": "Z-1877-2013",
      "product_description": "Carestream DRX Evolution System, X-Ray System ---  The DRX-Evolution system is a permanently installed diagnostic x-ray system for generation of x-rays for examination of various anatomical regions.",
      "product_quantity": "US: 49 units; Foreign: 183 units (revised)",
      "reason_for_recall": "Due to potential for an x-ray exposure technique change.",
      "recall_initiation_date": "20130603",
      "center_classification_date": "20130812",
      "termination_date": "20140129",
      "report_date": "20130821",
      "code_info": "Carestream DRX Evolution Systems using V5.5.410.33 MR2 Software",
      "more_code_info": ""
    }
  ]
}