# FDA recall Z-0209-2024

> **Abbott** · Class II · device recall initiated 2023-09-28.

## Product

Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator

## 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.

## Distribution

US, Taiwan, and Colombia

## Key facts

- **Recall number:** Z-0209-2024
- **Recalling firm:** Abbott
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-28
- **Report date:** 2023-11-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Plymouth, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0209-2024

## Citation

> AI Analytics. FDA recall Z-0209-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0209-2024. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*