Drug recall
Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation
FDA recall event 93277 · Class II · Liberty Medical Solutions, LLC
Key facts
| Event ID | 93277 |
|---|---|
| Recall numbers | Z-0506-2024 |
| Recalling firm | Liberty Medical Solutions, LLC |
| Product type | Devices |
| Products | Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Nov 3, 2023 |
| Report date | Dec 13, 2023 |
| City | Tampa |
| State | FL |
| Country | United States |
| FEI number | 3012251759 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: