{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Glens Falls",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76347",
      "recalling_firm": "Angiodynamics Inc. (Navilyst Medical Inc.)",
      "address_1": "10 Glens Falls Tech Park",
      "address_2": "N/A",
      "postal_code": "12801-3864",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "CA, KY, MD, OR, VA, TX",
      "recall_number": "Z-1853-2017",
      "product_description": "NAMIC Fluid Delivery Set - 72\" (183cm) UPN H965913000051, Catalog 91300005",
      "product_quantity": "8 boxes/25 units",
      "reason_for_recall": "The product has the potential to be non-sterile as it was not packaged in accordance to specification.",
      "recall_initiation_date": "20170113",
      "center_classification_date": "20170418",
      "termination_date": "20180625",
      "report_date": "20170426",
      "code_info": "Lot Number: 5122528"
    }
  ]
}