Multi-Mode Stimulator — Class II medical device recall Z-0506-2024
Ongoing recall by Liberty Medical Solutions, LLC, reported 2023-12-13, distributed nationwide. The instruction manuals that were included with the Multi-Mode Stimulators distributed from 2018 to 2023 did n
| Recall number | Z-0506-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Liberty Medical Solutions, LLC, Tampa, FL, United States |
| Recall initiated | 2023-11-03 |
| Classified | 2023-12-07 |
| Reported by FDA | 2023-12-13 |
| Distributed | Nationwide (US) |
| Quantity | 473 units |
| UPC / GTIN / UDI-DI | 00860000178303 |
| Serial numbers | 150900416, 151100129, 151100395, 160107746, 160107747, 160107752, 160107762, 160107764, 160107765, 160107772, 160700121, 160700386, 160700398, 160700407, 160800065, 160800066, 160800067, 160800068, 160800069, 160800070, 160800072, 160800075, 160800076, 160800079, 160800080 and 446 more |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0506-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.