LIBERTY MEDICAL SOLUTIONS, LLC
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (3)
Devices registered here (3)
- Interferential Current TherapyProduct code LIH (opens in a new tab) · Class II · Neurology · 21 CFR 882.5890
- Stimulator, Nerve, Transcutaneous, For Pain ReliefProduct code GZJ (opens in a new tab) · Class II · Neurology · 21 CFR 882.5890
- Stimulator, Muscle, PoweredProduct code IPF (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.5850
Recalls & enforcement
- Class IIOngoing2023-11-03The 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.
FDA inspections (3)
- VAI2026-06-04Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- NAI2023-08-23No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
- NAI2018-06-11No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “LIBERTY MEDICAL SOLUTIONS, LLC (FEI 3012251759) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3012251759-liberty-medical-solutions-llc/
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