{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "cfres_id": "36093",
      "product_res_number": "Z-0298-05",
      "event_date_initiated": "2004-07-28",
      "event_date_posted": "2004-12-08",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-12-17",
      "res_event_number": "30552",
      "product_code": "MIE",
      "product_description": "CryoValve, Pulmonary Valve & Conduit",
      "code_info": "Donor #75387, Serial #8235992, Model #PV00",
      "firm_fei_number": "3001451326",
      "recalling_firm": "Cryolife Inc",
      "address_1": "1655 Roberts Blvd Nw",
      "city": "Kennesaw",
      "state": "GA",
      "postal_code": "30144-3632",
      "additional_info_contact": "Mr. P. Tyler Cochran, CQA, CTBS\n770-419-3355",
      "reason_for_recall": "CryoLife received information stating that the tissue donation was deferred due to possible Hepaititis C suspected by the MD.",
      "root_cause_description": "Other",
      "action": "Consignee was notified verbally on 07/28/2004. The Allograft was retrieved and discarded.",
      "product_quantity": "1 tissue",
      "distribution_pattern": "MI",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}