{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "211119",
      "product_res_number": "Z-0524-2025",
      "event_date_initiated": "2024-08-08",
      "event_date_posted": "2024-12-03",
      "recall_status": "Open, Classified",
      "res_event_number": "95757",
      "product_code": "RHK",
      "product_description": "Fusion Pro 24, Model 17000",
      "code_info": "Model 17000\n Product Report Accession Number: 2021046-000",
      "firm_fei_number": "3003468623",
      "recalling_firm": "Epilog Laser Corp.",
      "address_1": "16371 Table Mountain Pkwy",
      "city": "Golden",
      "state": "CO",
      "postal_code": "80403-1826",
      "additional_info_contact": "Zachary Steadman\n303-277-1188",
      "reason_for_recall": "a. A small number of Fusion Pro 24 units were released with an incorrectly placed Interlock device. As a result, the system can be operated with the front-loading door in an open position.\nb. Fails to comply with Class 2 designation, indicated in Part 6 of Laser Product Report. An incorrectly placed Interlock device can allow Class 4 laser radiation fields during operation.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "The measures to be taken to repair such defect or to bring the product into\ncompliance with the Federal standard.\nThis Recall provides corrections by repair to a defective safety interlock location by a kit with comprehensive instructions, offered at no cost to purchasers",
      "product_quantity": "751",
      "distribution_pattern": "US Nationwide Distribution",
      "openfda": {
        "device_name": "Laser Marker Or Engraver, Industrial Or Commercial",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}