{
  "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,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "cfres_id": "35342",
      "product_res_number": "Z-0026-05",
      "event_date_initiated": "2004-07-15",
      "event_date_posted": "2004-10-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-12-31",
      "res_event_number": "30191",
      "product_code": "MIE",
      "product_description": "CryoValve, Pulmonary Valve & Conduit",
      "code_info": "Donor Number: 68668, Serial Number: 8037696, 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": "A pre-implant swab culture of the aortic valve, which was procured from the same donor, was positive for Methicillin resistant Staphyococcus aureus.",
      "root_cause_description": "Other",
      "action": "The physician was notified by letter on 07/15/2004.",
      "product_quantity": "1 tissue",
      "distribution_pattern": "The tissue was shipped to one physician in CA.",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}