{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "29085",
      "product_res_number": "Z-0019-04",
      "event_date_initiated": "2003-08-18",
      "event_date_posted": "2003-10-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-10-15",
      "res_event_number": "27051",
      "product_code": "MIE",
      "product_description": "CryoValve, Pulmonary Valve & Conduit SG",
      "code_info": "Donor #61354, Device #7693941, Model #SGPV00",
      "firm_fei_number": "3001451326",
      "recalling_firm": "Cryolife Inc",
      "address_1": "1655 Roberts Blvd Nw",
      "city": "Kennesaw",
      "state": "GA",
      "postal_code": "30144",
      "additional_info_contact": "Sylvie L. Verdon\n770-419-3355",
      "reason_for_recall": "The heart valve procurement exceeded the warm ischemic time criteria.",
      "root_cause_description": "Other",
      "action": "The physician was notified by letter on 8/18/2002. The tissue was reported implanted on 4/08/2003.",
      "product_quantity": "1 unit",
      "distribution_pattern": "Tissue was distributed to one physician in CA.",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}