Class II — Liberty Medical Solutions, LLC
| Recalling firm | Liberty Medical Solutions, LLC |
|---|---|
| Registered facility | LIBERTY MEDICAL SOLUTIONS, LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | 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 |
| Quantity | 473 units |
| Distribution | US Nationwide distribution in the states of CT, FL, NC, NJ, NY. |
| Initiated | 2023-11-03 |
| Classified | 2023-12-07 |
| Recall number | Z-0506-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Liberty Medical Solutions, LLC (Z-0506-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93277/
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