Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

NeuroTherm NT2000iX Radiofrequency (RF) Generator Recalled by Abbott Laboratories Inc. (St Jude Medical) Due to Potential capacitor failure which typically manifests as in...

Date: April 22, 2021
Company: Abbott Laboratories Inc. (St Jude Medical)
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Abbott Laboratories Inc. (St Jude Medical) directly.

Affected Products

NeuroTherm NT2000iX Radiofrequency (RF) Generator, Model Number RFG-NT-2000

Quantity: 318 units

Why Was This Recalled?

Potential capacitor failure which typically manifests as in inability to provide output on one or more channels. In some instances, users reported a charring/smoky odor or emission.

Where Was This Sold?

US and AUSTRALIA, EGYPT, SOUTH AFRICA, BELGIUM, COLOMBIA, UNITED KINGDOM, COSTA RICA, ISRAEL, SOUTH KOREA, SINGAPORE, TAIWAN

About Abbott Laboratories Inc. (St Jude Medical)

Abbott Laboratories Inc. (St Jude Medical) has 5 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report