{
  "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
    }
  },
  "results": [
    {
      "cfres_id": "52017",
      "product_res_number": "Z-0842-2007",
      "event_date_initiated": "2007-04-17",
      "event_date_posted": "2007-06-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-12-31",
      "res_event_number": "37876",
      "product_code": "MIE",
      "product_description": "Aortic Valve & Conduit",
      "code_info": "Donor number 87980, Serial number 8892143, Model Number 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": "Bryan Brosseau\n770-419-3355",
      "reason_for_recall": "Donor tissue was released prior to information received regarding a pericardial effusion.",
      "root_cause_description": "Other",
      "action": "Both physicians were contacted by telephone on 4/17 & 18/2007. Both tissues were returned to CryoLife",
      "product_quantity": "1 tissue",
      "distribution_pattern": "AZ, CO",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}