# FDA recall Z-0506-2024

> **Liberty Medical Solutions, LLC** · Class II · device recall initiated 2023-11-03.

## Product

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.

## Distribution

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

## Key facts

- **Recall number:** Z-0506-2024
- **Recalling firm:** Liberty Medical Solutions, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-03
- **Report date:** 2023-12-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tampa, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0506-2024

## Citation

> AI Analytics. FDA recall Z-0506-2024. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-0506-2024. Source: US FDA. Licensed CC0.

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