{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "203550",
      "product_res_number": "Z-0209-2024",
      "event_date_initiated": "2023-09-28",
      "event_date_posted": "2023-11-02",
      "recall_status": "Open, Classified",
      "res_event_number": "93152",
      "product_code": "GXD",
      "k_numbers": [
        "K111576"
      ],
      "product_description": "Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator",
      "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",
      "firm_fei_number": "3005334138",
      "recalling_firm": "Abbott",
      "address_1": "5050 Nathan Ln N",
      "city": "Plymouth",
      "state": "MN",
      "postal_code": "55442-3209",
      "additional_info_contact": "Shelley Lange\n651-756-4091",
      "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.",
      "root_cause_description": "Process change control",
      "action": "Abbott issued an URGENT:  MEDICAL DEVICE RECALL notice to its consignees on 09/28/2023 via FedEx 2nd day delivery.  The notice explained the problem, risk, and requested return of the device for inspection.  Those devices which pass, will be returned.  Should your device(s) fail the inspection, your local Abbott Representative can advise the consignee of alternate commercially available products.",
      "product_quantity": "34 devices",
      "distribution_pattern": "US, Taiwan, and Colombia",
      "openfda": {
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        ],
        "device_name": "Generator, Lesion, Radiofrequency",
        "medical_specialty_description": "Neurology",
        "regulation_number": "882.4400",
        "device_class": "2"
      }
    }
  ]
}