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Liberty Medical Solutions, LLC recalls Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation
Recalled December 13, 2023 · FDA recall Z-0506-2024 · Liberty Medical Solutions
Hazard
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. · FDA Class II
Units
473 units
Sold at
US Nationwide distribution in the states of CT, FL, NC, NJ, NY.
Description
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.
Product
Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation
Manufacturer(s)
Liberty Medical Solutions, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →