Reported Dec 13, 2023 · Ongoing
Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation
Liberty Medical Solutions, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Liberty Medical Solutions, LLC · 3653 Madaca Ln · Tampa, FL · 33618-2048
Is this the product you have?
- Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation
- Lot codes and dates
- UDI/DI 00860000178303
- Serial Numbers
473 of 473 codes
181102627180101759180302368180603258180101748180603502160700386170305821170305701180603845SZ151100022180603489SZ160801811180603829151100395180101912181102643160800430180603799160800489181102635181102714180302357181102642161202284160800483180603914180101917161202293161202285181102649160107765180603065180603924SZ160502068180603841180603864160800092180603059160800417SZ160700097170305806160800493161202287181102646181102789180101911SZ151100005180603839SZ151100017181102803180101738160800429180302376180603041160800508180603958180603965180603822180603244
- Amount recalled
- 473 units
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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