{
  "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,
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  "results": [
    {
      "cfres_id": "36630",
      "product_res_number": "Z-0581-05",
      "event_date_initiated": "2004-12-17",
      "event_date_posted": "2005-03-10",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-01-27",
      "res_event_number": "30803",
      "product_code": "MIE",
      "product_description": "CryoValve, Aortic Valve and Conduit",
      "code_info": "Donor #62654, Serial #7816174, Model #AV00",
      "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\n770-419-3355",
      "reason_for_recall": "Records noted that the infant donor's mother had tested positive for Hepatitis B.",
      "root_cause_description": "Other",
      "action": "Physicians were notified by letter on 12/17/2004.",
      "product_quantity": "1 tissue",
      "distribution_pattern": "CA, FL",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
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}