{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Golden",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95757",
      "recalling_firm": "Epilog Laser Corp.",
      "address_1": "16371 Table Mountain Pkwy",
      "address_2": "",
      "postal_code": "80403-1826",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0524-2025",
      "product_description": "Fusion Pro 24, Model 17000",
      "product_quantity": "751",
      "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.  b. 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.",
      "recall_initiation_date": "20240808",
      "center_classification_date": "20241203",
      "report_date": "20241211",
      "code_info": "Model 17000  Product Report Accession Number: 2021046-000",
      "more_code_info": ""
    }
  ]
}