{
  "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": "Bloomington",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72965",
      "recalling_firm": "Cook Medical Incorporated",
      "address_1": "400 N Daniels Way",
      "address_2": "N/A",
      "postal_code": "47404-9155",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Worldwide",
      "recall_number": "Z-0689-2016",
      "product_description": "Zilver¿ 518RX Vascular Stent with Rapid Exchange Delivery System",
      "product_quantity": "753",
      "reason_for_recall": "Manufacturing of the joint between the inner catheter and stylet of the delivery system does not consistently meet specifications, and the joint may separate during deployment. Failure of this joint during a procedure may result in a partial stent deployment. The clinical effect of a partial deployment may be a need for surgical intervention, or may result in vessel trauma or an embolic event",
      "recall_initiation_date": "20151222",
      "center_classification_date": "20160122",
      "termination_date": "20170725",
      "report_date": "20160203",
      "code_info": "Catalog Prefix ZIVX5. All Lots"
    }
  ]
}