{
  "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": "Largo",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63009",
      "recalling_firm": "Linvatec Corp. dba ConMed Linvatec",
      "address_1": "11311 Concept Blvd",
      "address_2": "N/A",
      "postal_code": "33773-4908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and the countries of Canada, DK, HK, IN, IT, KR, MY, RU, CO, VN, ZA.",
      "recall_number": "Z-2455-2012",
      "product_description": "***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source",
      "product_quantity": "1",
      "reason_for_recall": "Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of their products LS7700 Xenon Universal Light Source and LS7600 Xenon Light Source are intended to be used with an endoscope to provide illumination during endoscopic procedures.",
      "recall_initiation_date": "20110520",
      "center_classification_date": "20120925",
      "termination_date": "20120926",
      "report_date": "20121003",
      "code_info": "GCT",
      "more_code_info": ""
    }
  ]
}