Abbott: Medical Device Recall in 2023 - (Recall #: Z-0209-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 28, 2023

Date Posted: November 8, 2023

Recall Number: Z-0209-2024

Event ID: 93152

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.

Status: Ongoing

Product Quantity: 34 devices

Code Information:

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

Distribution Pattern:

US, Taiwan, and Colombia

Voluntary or Mandated:

Voluntary: Firm initiated