{
  "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": {
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  "results": [
    {
      "cfres_id": "31958",
      "product_res_number": "Z-0855-04",
      "event_date_initiated": "2004-02-25",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-09-14",
      "res_event_number": "28467",
      "product_code": "MIE",
      "product_description": "CryoValve Conduit and Pulmonary Valve and Conduit",
      "code_info": "Donor #71899, Serial #8080113, 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": "A retrospective review of donor files conducted by CryoLife revealed an expired solution had been used during processing of the associated tissues.",
      "root_cause_description": "Other",
      "action": "Consignees were notified by letter on 03/02/2004.",
      "product_quantity": "1 unit",
      "distribution_pattern": "CA",
      "openfda": {
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        "medical_specialty_description": "Unknown",
        "regulation_number": "",
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}