{
  "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": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97792",
      "recalling_firm": "Covidien, LP",
      "address_1": "60 Middletown Ave",
      "address_2": "",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Austria, Belgium, Chile, Estonia, Finland, France, Germany, Greece, Hungary, Israel, Italy, Japan, Kuwait, Malaysia, Netherlands, Poland, Portugal, Romania, Saudi Arabia, Slovakia, Spain, United Kingdom.",
      "recall_number": "Z-0486-2026",
      "product_description": "Covidien Signia\" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin);  BOX LOBECTOMIA VATS 3D;  CFN: BOX06170V4;",
      "product_quantity": "2 units (OUS only)",
      "reason_for_recall": "A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for uncontrolled motion.",
      "recall_initiation_date": "20250925",
      "center_classification_date": "20251107",
      "report_date": "20251119",
      "code_info": "CFN: BOX06170V4; UDI-DI: 00763000988975; Lot numbers: 0231961695;",
      "more_code_info": ""
    }
  ]
}