---
title: "Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning gen... — FDA record Z-0209-2024 | Is It on Recall"
description: "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 result"
url: https://isitonrecall.com/recall/fda-device-z-0209-2024-abbott-nt2000ix-radiofrequency-rf-generator-ref-rfg-nt-2000-lesioning-generator/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator — FDA record Z-0209-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 28, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator
- **Reason**: 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.
- **Classification**: Class II
- **Recalling firm**: Abbott
- **Quantity**: 34 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0209-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0209-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 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 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US, Taiwan, and Colombia

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Nov 8, 2023
- **Recall initiation date**: Sep 28, 2023
- **Center classification date**: Nov 2, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0209-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Abbott records](https://isitonrecall.com/brand/abbott/)