PlainRecalls
FDA Devices Moderate Class II Ongoing

Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation

Reported: December 13, 2023 Initiated: November 3, 2023 #Z-0506-2024

Product Description

Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation

Reason for Recall

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.

Details

Units Affected
473 units
Distribution
US Nationwide distribution in the states of CT, FL, NC, NJ, NY.
Location
Tampa, FL

Frequently Asked Questions

What product was recalled?
Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation. Recalled by Liberty Medical Solutions, LLC. Units affected: 473 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 13, 2023. Severity: Moderate. Recall number: Z-0506-2024.