{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "32163",
      "product_res_number": "Z-0389-04",
      "event_date_initiated": "2004-05-10",
      "event_date_created": "2015-06-25",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-10-06",
      "res_event_number": "28581",
      "product_description": "Lodox Statscan digital radiographic system.",
      "code_info": "Serial numbers LDX002 and LDX004.",
      "firm_fei_number": "3004035693",
      "recalling_firm": "Lodox Na Llc",
      "address_1": "23360 Clarkshire Dr",
      "city": "South Lyon",
      "state": "MI",
      "postal_code": "48178-8920",
      "additional_info_contact": "William Greenway\n248-446-8480",
      "reason_for_recall": "The labels do not have proper identification and certification and the firm failed to provide adequate test and quality control procedures to establish certification by the manufacturer.",
      "root_cause_description": "Other",
      "action": "The device in Illinois was re-exported.  The device in Maryland was tested on 5/10/04 by a trained Lodox representative and proper labeling was reportedly attached.",
      "product_quantity": "2",
      "distribution_pattern": "Illinois and Maryland.",
      "openfda": {}
    }
  ]
}