{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Kennesaw",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88929",
      "recalling_firm": "CryoLife, Inc.",
      "address_1": "1655 Roberts Blvd Nw",
      "address_2": "",
      "postal_code": "30144-3632",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution in the European Union only (Germany/Switzerland)",
      "recall_number": "Z-0384-2022",
      "product_description": "BioGlue Surgical Adhesive, Model BG3510-5-G",
      "product_quantity": "156 5-pack box units",
      "reason_for_recall": "Product is not approved for use in the EU and should not have been distributed in the EU.",
      "recall_initiation_date": "20211007",
      "center_classification_date": "20211215",
      "termination_date": "20231023",
      "report_date": "20211222",
      "code_info": "Model BG3510-5-G, Lot BG000255",
      "more_code_info": ""
    }
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}