{
  "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": "Westford",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69463",
      "recalling_firm": "Cynosure, Inc.",
      "address_1": "5 Carlisle Rd",
      "address_2": "N/A",
      "postal_code": "01886",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - Nationwide Distribution and the countries of : Australia, Canada, France, Germany, Italy, Netherlands, Ukraine and UK.",
      "recall_number": "Z-0169-2015",
      "product_description": "Elite XPL (Pulsed Light) Handpiece for the Cynosure Elite MPX Laser System",
      "product_quantity": "322 units",
      "reason_for_recall": "If the laser system is turned on and the user adjusts, installs or removes the XPL pulsed light handpiece, there is a potential risk of an electrical shock",
      "recall_initiation_date": "20141009",
      "center_classification_date": "20141104",
      "termination_date": "20150326",
      "report_date": "20141112",
      "code_info": "All Serial numbers"
    }
  ]
}