{
  "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": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93152",
      "recalling_firm": "Abbott",
      "address_1": "5050 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-3209",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US, Taiwan, and Colombia",
      "recall_number": "Z-0209-2024",
      "product_description": "Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator",
      "product_quantity": "34 devices",
      "reason_for_recall": "Certain NT2000iX RF generators were serviced using a tool that was subsequently found to be out of tolerance and therefore may not have provided accurate results for potential capacitance failure.",
      "recall_initiation_date": "20230928",
      "center_classification_date": "20231102",
      "report_date": "20231108",
      "code_info": "UDI/DI 05415067022417, serial numbers:  16930509, 16983330, 17583407, 17634837, 17783928, 17783930, 17905961, 17928413, 17954521, 17991999, 18047384, 18493711, 18522937, 18675068, 18690920, 18709734, 18742997, 2475-12, 2504-12, 2547-13, 2885-14, 3003-14, 3278-15, 3450-15, 3550-15, 17942357, 18003310, 18102335, 18132017, 18132092, 18657521, 18666647, 19182119, 19197174"
    }
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}