{
  "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": "Glens Falls",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84072",
      "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": "The products were distributed to the following US states:  LA, MA, OR, VA, and WA.",
      "recall_number": "Z-0411-2020",
      "product_description": "Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI Semi-Flex Electrosurgical Device, Part Number H7877001026151",
      "product_quantity": "30",
      "reason_for_recall": "The devices are not labelled correctly.  End users impacted by this issue may experience a procedural delay.",
      "recall_initiation_date": "20191002",
      "center_classification_date": "20191115",
      "termination_date": "20200729",
      "report_date": "20191127",
      "code_info": "Lot 5476032"
    }
  ]
}