{
  "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": "83334",
      "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": "Telephone",
      "distribution_pattern": "The products were distributed to the following US states:  DC, IL, IN, MI, NJ, TN, TX, and WI.",
      "recall_number": "Z-2444-2019",
      "product_description": "AngioDynamics VenaCure EVLT NeverTouch Procedure Kit, 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG, Catalog Number 11403012",
      "product_quantity": "109",
      "reason_for_recall": "The affected product is properly labelled with an expiration date of March 31, 2022; but the RFID programmed expiration date is April-2014 which results in an error message when connected to the laser source and prevents the product from being used.",
      "recall_initiation_date": "20190627",
      "center_classification_date": "20190830",
      "termination_date": "20200729",
      "report_date": "20190911",
      "code_info": "Lot 5456490; UPN H787114030120"
    }
  ]
}