{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bloomington",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96703",
      "recalling_firm": "Cook Incorporated",
      "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": "Worldwide distribution - US Nationwide and the countries of Belgium, Germany, Spain, France, Ireland, Italy Netherlands, Switzerland, South Africa, Slovenia.",
      "recall_number": "Z-1787-2025",
      "product_description": "Check=Flo Performer Introducer, 14.0Fr, Reference Part Number(RPN)  REF RCFW-14.0-0-38-30-RB, Order Number (GPN) REF G08957,",
      "product_quantity": "89 units",
      "reason_for_recall": "Cook Medical identified that devices from the affected device lots may contain the incorrectly sized introducer sheath.",
      "recall_initiation_date": "20250417",
      "center_classification_date": "20250516",
      "report_date": "20250528",
      "code_info": "UDI/DI 00827002089570, Lot Number 16376242"
    }
  ]
}