RegWardenFDA facility compliance records
Facility

LIBERTY MEDICAL SOLUTIONS, LLC

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2018: 1 inspections; 2023: 1 recalls, 1 inspections; 2026: 1 inspections2017120182019202020212022220232024202512026
  • Recalls (1)
  • Inspections (3)

Devices registered here (3)

Recalls & enforcement

  • Class IIOngoing2023-11-03
    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.

FDA inspections (3)

  • VAI2026-06-04
    Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
  • NAI2023-08-23
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
  • NAI2018-06-11
    No 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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