FDANovember 3, 2023device

Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

liberty medical solutionslibertyliberty medical

UPCs

00860000178303

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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