{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86826",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Foreign distribution only - Canada.",
      "recall_number": "Z-0782-2021",
      "product_description": "Greffe Aorte-LF (product info is in French); Model DYNJ31877F - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.",
      "product_quantity": "45",
      "reason_for_recall": "The cylindrical sponge component is not x-ray detectable.",
      "recall_initiation_date": "20201113",
      "center_classification_date": "20210107",
      "termination_date": "20211026",
      "report_date": "20210113",
      "code_info": "Lot 20FBW645 (Expiration: 02/28/2022); Lot 20HBM397 (Expiration: 02/28/2022)",
      "more_code_info": ""
    }
  ]
}