{
  "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": [
    {
      "country": "United States",
      "city": "Miami Lakes",
      "address_1": "14201 Nw 60th Ave",
      "reason_for_recall": "Inability to deploy the stent or partial stent deployment.",
      "address_2": "",
      "product_quantity": "4,400 units in US; 3,100 units to Foreign Countries",
      "code_info": "Catalog Number:  P05030RXB, Lot Number: 17241836; Catalog Number: P09030RXB, Lot Number:  17241838; Catalog Number: P07030RXB, Lot Number : 17291878;  Catalog Number: P07040RXB, Lot Number:  17291879;  Catalog Number: P06040RXB, Lot Number:  17415243.",
      "center_classification_date": "20160610",
      "distribution_pattern": "NATIONWIDE and FOREIGN CONSIGNEES: Japan, Taiwan, Thailand and South Korea.",
      "state": "FL",
      "product_description": "Cordis PRECISE (R)  RX Nitinol Stent System (Biliary)",
      "report_date": "20160622",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cordis Corporation",
      "recall_number": "Z-1947-2016",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "74097",
      "termination_date": "20190726",
      "more_code_info": "",
      "recall_initiation_date": "20160504",
      "postal_code": "33014-2802",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}