Class II — Potential Health Hazard

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

Multi-Mode Stimulator Recalled by Liberty Medical Solutions, LLC Due to The instruction manuals that were included with the...

Date: November 3, 2023
Company: Liberty Medical Solutions, LLC
Status: Ongoing
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 Liberty Medical Solutions, LLC directly.

Affected Products

Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation

Quantity: 473 units

Why Was This Recalled?

The instruction manuals that were included with the Multi-Mode Stimulators distributed from 2018 to 2023 did not contain all of the appropriate warnings and contraindications.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Liberty Medical Solutions, LLC

Liberty Medical Solutions, LLC has 1 total recall tracked by RecallDetector.

Related Recalls

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