{
  "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": "2026-08-22",
    "results": {
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  "results": [
    {
      "cfres_id": "31330",
      "product_res_number": "Z-0530-04",
      "event_date_initiated": "2004-01-16",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-09-03",
      "res_event_number": "28176",
      "product_code": "MIE",
      "product_description": "CryoValve, Aortic Valve & Conduit",
      "code_info": "Donor #69666, Serial #8008559, 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, CQA, CTBS\n770-419-3355",
      "reason_for_recall": "Microorganisms were detected in associated tissue.",
      "root_cause_description": "Other",
      "action": "Consignees were notified by letter on 1/16/2004.",
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}