{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "27435",
      "product_res_number": "Z-0861-03",
      "event_date_initiated": "2003-05-05",
      "event_date_posted": "2003-05-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-07-17",
      "res_event_number": "26286",
      "product_code": "MIE",
      "product_description": "CryoValve Allograft, Pulmonary Heart valve & Conduit.",
      "code_info": "Model #PV00, Serial #7916346",
      "firm_fei_number": "3001451326",
      "recalling_firm": "Cryolife Inc",
      "address_1": "1655 Roberts Blvd Nw",
      "city": "Kennesaw",
      "state": "GA",
      "postal_code": "30144",
      "additional_info_contact": "Shari L. Allen\n770-419-3355",
      "reason_for_recall": "Microorganisms were detected in associated allografts after initial release of donor.",
      "root_cause_description": "Other",
      "action": "The implanting physician was notified via letter on May 5, 2003. Allograft was reported implanted 1/17/2003.",
      "product_quantity": "1 unit",
      "distribution_pattern": "Allograft was distributed to and implanted by one physician in California.",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}