{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Kennesaw",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77369",
      "recalling_firm": "CryoLife, Inc.",
      "address_1": "1655 Roberts Blvd NW",
      "address_2": "N/A",
      "postal_code": "30144-3632",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product distributed in Japan.",
      "recall_number": "Z-2623-2017",
      "product_description": "BioGlue Surgical Adhesive, Model/Catalog Number BG3510-5-J",
      "product_quantity": "705 single pack boxes",
      "reason_for_recall": "The courtesy labels in 9 boxes of BioGlue were incorrectly labeled as lot 17MJX007 instead of lot 17MJX002.",
      "recall_initiation_date": "20170519",
      "center_classification_date": "20170623",
      "termination_date": "20190208",
      "report_date": "20170705",
      "code_info": "Lot Code 17MJX002, Model/Catalog Number BG3510-5-J"
    }
  ]
}