{
  "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": "36910",
      "product_res_number": "Z-0669-05",
      "event_date_initiated": "2005-01-12",
      "event_date_posted": "2005-04-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-04-12",
      "res_event_number": "30971",
      "product_code": "MIE",
      "product_description": "CryoValve, Pulmonary Valve and Conduit",
      "code_info": "Donor Number: 70022, Serial Number: 8056613, Model Number: 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": "During a retrospective review CryoLife's Medical Director identified pre-processing and incoming bioburden cultures of the heart tissue, which detected Staphylococcus aureas.",
      "root_cause_description": "Other",
      "action": "Consignee was notified by letter on 01/12/2005.",
      "product_quantity": "1 tissue",
      "distribution_pattern": "KS",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
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}