{
  "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": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96294",
      "recalling_firm": "Smiths Medical ASD, Inc.",
      "address_1": "6000 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution.",
      "recall_number": "Z-1286-2025",
      "product_description": "smiths medical ProPort Plastic Venous Access System, Implantable Venous Access Systems, 82-24",
      "product_quantity": "0 units",
      "reason_for_recall": "The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.",
      "recall_initiation_date": "20250213",
      "center_classification_date": "20250318",
      "report_date": "20250326",
      "code_info": "UDI/DI 10610586012754, Lot Numbers:  4196769"
    }
  ]
}