PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: November 8, 2023 Initiated: September 28, 2023 #Z-0209-2024

Product Description

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.

Details

Recalling Firm
Abbott
Units Affected
34 devices
Distribution
US, Taiwan, and Colombia
Location
Plymouth, MN

Frequently Asked Questions

What product was recalled?
Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator. Recalled by Abbott. Units affected: 34 devices.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 8, 2023. Severity: Moderate. Recall number: Z-0209-2024.