{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Queensbury",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90811",
      "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 in the states of FL, NC, NJ, NM, NY, PA, TX, VA.",
      "recall_number": "Z-1819-2022",
      "product_description": "VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM    Ref./ Catalog No.: EVLT55OPS (each box contains 5 Procedure Kits). For use in the treatment of varicose veins.",
      "product_quantity": "40 units",
      "reason_for_recall": "OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not meet the required dimensional specification, may result in damage to the sheath, including separation or the inability to move the fiber within the sheath. A damaged sheath will necessitate removal from the patient, which may result in procedural delay and/or surgical intervention",
      "recall_initiation_date": "20220810",
      "center_classification_date": "20220927",
      "report_date": "20221005",
      "code_info": "UDI-DI: 25051684014653 UPN: H787EVLT55OPS5 Lot Number: 5728621"
    }
  ]
}