{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "cfres_id": "39204",
      "product_res_number": "Z-0859-05",
      "event_date_initiated": "2005-05-17",
      "event_date_posted": "2005-06-01",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-06-01",
      "res_event_number": "32127",
      "product_code": "MIE",
      "product_description": "Aortic Valve & Conduit",
      "code_info": "Donor #77647, Serial #8461379, Model #AV00",
      "firm_fei_number": "3001451326",
      "recalling_firm": "Cryolife Inc",
      "address_1": "1655 Roberts Blvd Nw",
      "city": "Kennesaw",
      "state": "GA",
      "postal_code": "30144-3632",
      "reason_for_recall": "Subsequent to tissue release, CryoLife received new information related to the donor time of death, which caused the donor to no longer meet CryoLife's acceptance criteria for warm ischemic time.",
      "root_cause_description": "Other",
      "action": "Consignees were notified by telephone on May 17, 2005. Both tissues were returned and destroyed.",
      "product_quantity": "1 unit",
      "distribution_pattern": "IL, MT",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}