{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66133",
      "recalling_firm": "Lumenis, Inc.",
      "address_1": "3959 W 1820 S",
      "address_2": "N/A",
      "postal_code": "84104",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of  NJ, PA, and IL.",
      "recall_number": "Z-2191-2013",
      "product_description": "Vision One Laser System Model GA-0025020, Serial No: 10050, 10051, 10053.    Intended for use in the treatment of ocular pathology.",
      "product_quantity": "3 units",
      "reason_for_recall": "Lumenis has initiated a recall on certain models of Vision One System due to a potential for unintended laser exposure to the user.",
      "recall_initiation_date": "20130819",
      "center_classification_date": "20130911",
      "termination_date": "20131219",
      "report_date": "20130918",
      "code_info": "Model: GA-0025020",
      "more_code_info": ""
    }
  ]
}