{
  "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": "73163",
      "recalling_firm": "Cook Inc.",
      "address_1": "750 N Daniels Way",
      "address_2": "N/A",
      "postal_code": "47404-9120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of CA, FL, OK, OH, MI, TX, NJ, and NY.",
      "recall_number": "Z-0865-2016",
      "product_description": "Flexor Check-Flo Introducer, Catheter introducer,   Catalog #: KCFW-6.0-35-70-RB-HFANL0-HC    Intended for introduction of balloons, closed and non-tapered end catheters or diagnostic and interventional devices",
      "product_quantity": "25",
      "reason_for_recall": "Incorrect packaging. Reports of packages labeled as 6.0Fr actually containing 5.0Fr devices.",
      "recall_initiation_date": "20160120",
      "center_classification_date": "20160224",
      "termination_date": "20161121",
      "report_date": "20160302",
      "code_info": "Catalog #:   KCFW-6.0-35-70-RB-HFANL0-HC    Lot:  6166304",
      "more_code_info": ""
    }
  ]
}