{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84454",
      "recalling_firm": "Abbott Medical",
      "address_1": "5050 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-3209",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "Worldwide Distributed - US Nationwide in sates of: FL, PA, NY, TX, MI CA, IL, NE, AL, NV, including PR and the countries of: Malaysia, Korea, Paraguay",
      "recall_number": "Z-0783-2020",
      "product_description": "Fast-Cath Trio HEMOSTASIS INTRODUCER, 14F, 4.6 mm, REF 406303",
      "product_quantity": "814 devices",
      "reason_for_recall": "Fast-Cath Trio Hemostasis Introducer devices contained 12F sized dilators and sheaths instead of the expected 14F devices.",
      "recall_initiation_date": "20191209",
      "center_classification_date": "20200107",
      "termination_date": "20201214",
      "report_date": "20200115",
      "code_info": "UDI:  (01)15414734203903(17)220731(10)7133555, Batch: 7133555"
    }
  ]
}