{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Kennesaw",
      "address_1": "1655 Roberts Blvd Nw",
      "reason_for_recall": "Serological testing for the donor was performed with a blood sample that may have been hemodiluted due to the administration of normal saline to the donor prior to death.",
      "address_2": "",
      "product_quantity": "One",
      "code_info": "Serial No. 10119759, Model SGPH00",
      "center_classification_date": "20140123",
      "distribution_pattern": "US distribution in CA.",
      "state": "GA",
      "product_description": "Pulmonary Hemi-Artery SG  Used in heart surgery",
      "report_date": "20140129",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CryoLife, Inc.",
      "recall_number": "Z-0809-2014",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "67182",
      "termination_date": "20140220",
      "more_code_info": "",
      "recall_initiation_date": "20131122",
      "postal_code": "30144-3632",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}