{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Horsholm",
      "state": "N/A",
      "country": "Denmark",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74189",
      "recalling_firm": "Ellipse A/S",
      "address_1": "Agern Alle 11",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution to the states of : NJ, PA, MI, CO, CA, FL, OK, NY, NH, CT, AZ and MO.",
      "recall_number": "Z-1698-2016",
      "product_description": "Ellipse ND: YAG Laser applicator for Ellipse Nordlys system    Medical Laser Products.",
      "product_quantity": "US - 25",
      "reason_for_recall": "Failure to provide the required instructions specifying a procedure and schedule for calibration of the measurement system.",
      "recall_initiation_date": "20160505",
      "center_classification_date": "20160609",
      "termination_date": "20160729",
      "report_date": "20160615",
      "code_info": "All serial numbers"
    }
  ]
}