FDA recall record

Liberty Medical Solutions Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation recall — FDA Z-0506-2024

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

Class IIclassification
Z-0506-2024official record ID
Dec 13, 2023report date

Recall record at a glance

Official recordZ-0506-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmLiberty Medical Solutions, LLC
Report dateDec 13, 2023
Recall initiation dateNov 3, 2023
Quantity473 units
LocationTampa, FL, United States

Official product description

Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation

Why the product 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.

Distribution information

US Nationwide distribution in the states of CT, FL, NC, NJ, NY.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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