{
  "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": [
    {
      "country": "United States",
      "city": "Alpharetta",
      "address_1": "5405 Windward Pkwy",
      "reason_for_recall": "Mismatch between the length of the RF electrode (probe) and the cannula (introducer),",
      "address_2": "",
      "product_quantity": "51 kits",
      "code_info": "Lot Number M5264D205",
      "center_classification_date": "20160811",
      "distribution_pattern": "Distributed in the states of CT, IL, MA, MI, NV, NH, NC, and  TX, and the country of Canada.",
      "state": "GA",
      "product_description": "Coolife Sinergy Radiofrequency Kit, SIK-17-75-4 (109971504); Kit used in conjunction with a Radiofrequency Generator to create radiofrequency lesions in nervous tissue.",
      "report_date": "20160817",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Halyard Health, Inc",
      "recall_number": "Z-2391-2016",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "74553",
      "termination_date": "20160908",
      "more_code_info": "",
      "recall_initiation_date": "20160616",
      "postal_code": "30004-3894",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}