{
  "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": "Kennesaw",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82380",
      "recalling_firm": "CryoLife, Inc.",
      "address_1": "1655 Roberts Blvd Nw",
      "address_2": "N/A",
      "postal_code": "30144-3632",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was shipped to Texas",
      "recall_number": "Z-1219-2019",
      "product_description": "CryoPatch SG Pulmonary Hemi-Artery Patch",
      "product_quantity": "1",
      "reason_for_recall": "The device is recalled due to donor ineligibility of released human tissue. The firm received information that the tissue donor's blood culture tested positive for Enterobacter cloacae.",
      "recall_initiation_date": "20161121",
      "center_classification_date": "20190425",
      "termination_date": "20190924",
      "report_date": "20190501",
      "code_info": "Model #: SGPHOO Serial #10685466"
    }
  ]
}