{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Queensbury",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91909",
      "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:  CA,CO, FL, IA, NY, OH",
      "recall_number": "Z-1381-2023",
      "product_description": "NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical ablation of soft tissue.  Catalog Number: 20400111  UPN: H787204001110",
      "product_quantity": "10 boxes( 5 probes/box)",
      "reason_for_recall": "Not programmed in accordance with specification. The programming affects the RFID function and does not  allow the NanoKnife probes to be recognized by the NanoKnife generator resulting in a delay in procedure",
      "recall_initiation_date": "20230302",
      "center_classification_date": "20230412",
      "report_date": "20230419",
      "code_info": "UDI-DI: 15051684029643 Lot Number: 5762110"
    }
  ]
}