{
  "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": "32129",
      "product_res_number": "Z-0746-04",
      "event_date_initiated": "2004-02-18",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-03-30",
      "res_event_number": "28558",
      "product_code": "MIE",
      "product_description": "CryoValve, Aortic Valve and Conduit",
      "code_info": "Donor #68607, Serial #8044081, 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": "CryoLife received additional information after release of tissue indicating the donor had repeatedly reactive test results for antibody to HCV (EIA) in 1995.",
      "root_cause_description": "Other",
      "action": "Consignees were notified by telephone on 02/18/2004.",
      "product_quantity": "1 unit",
      "distribution_pattern": "DC, TX",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
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}