{
  "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": [
    {
      "status": "Terminated",
      "city": "Kennesaw",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80199",
      "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": "AR, OH",
      "recall_number": "Z-2272-2018",
      "product_description": "Cryopatch SG Pulmonary Human Cardiac Branch, Catalog Number SGP020",
      "product_quantity": "1 unit",
      "reason_for_recall": "Devices, which met FDA and AATB eligibility criteria, were distributed.  Final autopsy and toxicology reports indicated the presence of morphine in the urine.",
      "recall_initiation_date": "20180514",
      "center_classification_date": "20180621",
      "termination_date": "20190329",
      "report_date": "20180627",
      "code_info": "Serial Number 10988328"
    }
  ]
}