{
  "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": "Utica",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71518",
      "recalling_firm": "ConMed Corporation",
      "address_1": "525 French Rd",
      "address_2": "N/A",
      "postal_code": "13502-5945",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US distribution in the states of FL, OH, and the country of Spain.",
      "recall_number": "Z-0205-2016",
      "product_description": "Arthroscopic Energy 50¿ Probe with Suction, Catalog number: AES-50S    Peoduct Usage:  For resection, ablation, and coagulation of soft tissue and hemostasis of blood vessels in arthroscopic and orthopedic surgical procedures.",
      "product_quantity": "276 devices",
      "reason_for_recall": "Probe programming error.  The incorrect program can generate more heat at the surgical site, resulting in an elevated probability of tissue damage.",
      "recall_initiation_date": "20150617",
      "center_classification_date": "20151103",
      "termination_date": "20170411",
      "report_date": "20151111",
      "code_info": "1412161, 1410201, 1410271, 1412121, and 1412081"
    }
  ]
}