{
  "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": "Ongoing",
      "city": "Miami Lakes",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88821",
      "recalling_firm": "Cordis Corporation",
      "address_1": "14201 NW 60th Ave",
      "address_2": "N/A",
      "postal_code": "33014-2802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of: CA, FL, IN, LA, OH, OK, TX and OUS distribution to country of Canada.",
      "recall_number": "Z-0216-2022",
      "product_description": "SMART FLEX 9x60 BIL, 80cm  The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.",
      "product_quantity": "9 units",
      "reason_for_recall": "There is a potential for distal tip dislodgement or separation.",
      "recall_initiation_date": "20211001",
      "center_classification_date": "20211112",
      "report_date": "20211124",
      "code_info": "Product Code: SF09060SB; Lot No. 253349",
      "more_code_info": ""
    }
  ]
}