RecallRadar

FDA Device recall Z-0209-2024

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

On 2023-11-08 the FDA classified a Class II recall of Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator by Abbott, citing 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 cap….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0209-2024
ClassificationClass II
Statusongoing
Initiated2023-09-28
Published2023-11-08
Last updated2026-09-13 11:56 UTC
CompanyAbbott
Distributionn/a

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.

Identifiers

code_info
UDI/DI 05415067022417, serial numbers: 16930509, 16983330, 17583407, 17634837, 17783928, 17783930, 17905961, 17928413,…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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0209-2024%22

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