{
  "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": "Queensbury",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86627",
      "recalling_firm": "Angiodynamics, Inc.",
      "address_1": "603 Queensbury Ave",
      "address_2": "N/A",
      "postal_code": "12804-7619",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution including in the states of AL, CT,  GA, FL.",
      "recall_number": "Z-0418-2021",
      "product_description": "Angiodynamics 5F Standard Micro-Introducer Kit - indicated for  percutaneous introduction of a guidewire or catheter into  the vascular system, Catalog Number: 06597035  UPN: H787065970355",
      "product_quantity": "32 kits",
      "reason_for_recall": "5F Micro-Introducer Kits may not contain the correct device, packaged with a 4F Sheath/Dilator component",
      "recall_initiation_date": "20201014",
      "center_classification_date": "20201105",
      "termination_date": "20211019",
      "report_date": "20201111",
      "code_info": "Lot Number: 5626935  Expiration Date: 08/31/2023"
    }
  ]
}