{
  "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": "Miami Lakes",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88112",
      "recalling_firm": "Cordis Corporation",
      "address_1": "14201 NW 60th Ave",
      "address_2": "",
      "postal_code": "33014-2802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of AR, AZ, FL, GA, IN, NC, NJ, and WV. The country of Canada.",
      "recall_number": "Z-2079-2021",
      "product_description": "Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices.",
      "product_quantity": "680 units",
      "reason_for_recall": "The product in the packaging is larger (both inner and outer diameter) than the labeling indicates.",
      "recall_initiation_date": "20210609",
      "center_classification_date": "20210715",
      "termination_date": "20230216",
      "report_date": "20210721",
      "code_info": "Catalog: 504-657A Lot 17919780: Exp. Date 12/31/2022 and Lot 17988227: Exp. Date 10/31/2023",
      "more_code_info": ""
    }
  ]
}