{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "40947",
      "product_res_number": "Z-0210-06",
      "event_date_initiated": "2003-11-19",
      "event_date_posted": "2005-11-30",
      "recall_status": "Terminated",
      "event_date_terminated": "2009-07-02",
      "res_event_number": "32850",
      "product_code": "MIE",
      "product_description": "CryoValve, Alt Aortic Valve & Conduit",
      "code_info": "Donor #30436, Serial #6230415, Model #AV05,  Donor #30676, Serial #6231586, Model #AV05",
      "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": "Previously released tissues no longer meet CryoLife's enhanced suitability release criteria because donors possessed a positive post processing microbiological culture of 'potentially pathogenic' organisms.",
      "root_cause_description": "Other",
      "action": "Consignees were notified by letter starting 11/17/2003.",
      "product_quantity": "2 units",
      "distribution_pattern": "AR, AZ, CA, CT, DC, FL, IL, LA, MN, NC, NH, NV, NY, TN, TX, UT,  and Germany.",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}