{
  "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": "65805",
      "recalling_firm": "Carestream Health, Inc.",
      "address_1": "150 Verona Street",
      "address_2": "N/A",
      "postal_code": "14608-1733",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) including the states of New York, Massachusetts, Pennsylvania, Illinois, Texas, California and Louisiana., and the countries of Australia, Canada, Finland, Italy, Switzerland and United Kingdom.",
      "recall_number": "Z-0090-2014",
      "product_description": "DRX Revolution Mobile X-Ray System, Model DRXR-1, Verona Street Rochester, NY 14608    Catalog Numbers 1019397, 1023415, 1023423 --- Made in USA by Carestream Health, Inc. 150     The device is designed to perform radiographic x-ray examinations on all pediatric and adult patients, in all patient treatment areas.",
      "product_quantity": "23 units installed total (11 domestically & 12 internationally)",
      "reason_for_recall": "During an audit, Carestream discovered a DRX-1 System that captured an image which displayed an artifact.  This issue was discovered in manufacturing.  It occurs when the DRX product console software is updated to v5.6b software and the detector is not calibrated before use.",
      "recall_initiation_date": "20130726",
      "center_classification_date": "20131031",
      "termination_date": "20160525",
      "report_date": "20131106",
      "code_info": "Serial numbers: U.S. - 134,152,173,174,200,205,222,312,349,353,412, Worldwide Serial numbers: 469, 445, 306, 410, 453, 204, 483, 300, 171, 218"
    }
  ]
}