{
  "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,
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  "results": [
    {
      "cfres_id": "43961",
      "product_res_number": "Z-0480-06",
      "event_date_initiated": "2006-01-27",
      "event_date_posted": "2006-02-04",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-04-04",
      "res_event_number": "34502",
      "product_code": "MIE",
      "product_description": "CryoValve, Pulmonary Valve & Conduit",
      "code_info": "Donor number 78142, Serial number 8306247, 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. Bryan Brosseau\n770-419-3355",
      "reason_for_recall": "Additional serological testing performed after distribution indicates the donor has a past Hepatitis B infection.",
      "root_cause_description": "Other",
      "action": "Physicians were notified by letter on 1/27/2006.",
      "product_quantity": "1 unit",
      "distribution_pattern": "NY",
      "openfda": {
        "device_name": "Heart-Valve, Allograft",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
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    }
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}