Liberty Multi-Mode Stimulator LMS 1000Recalls & reported problems
Liberty Medical Solutions, LLC · The Liberty Medical Solutions, LLC Multi-Mode Stimulator (MMS) (the Device) is a battery powered electrotherapy device intended for clinic and outpatient rehabilitative therapy, acute postoperative care and home use for patients suffering from a variety of chronic pain issues. Prescribed by a physician, it gives the clinician a variety of electrotherapy modes to treat a range of indications. The MMS is designed for clinician and patient ease of use and provides safe and effective dispensing of the desired electrotherapy treatment. The Intended Use Environment is Home Healthcare but the Device can also be used in a Chiropractic, Physical Therapy or Pain Management Clinic. The Device uses a tactile button user interface for control of the operating system and therapy amplitude settings. The Device has a liquid crystal character display which provides information to the user and displays the current therapy settings. The Device’s therapeutic output is transmitted through the patient lead wires to the cutaneous hydrogel electrodes affixed to the user’s skin. The energy generated by the Device is conveyed, via the patient lead wires and cutaneous electrodes, through the patients skin to excite either the underlying motor nerves to elicit involuntary muscle contractions or the sensory nerves to manage pain. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Nov 3, 2023Class IIOpen, Classified
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.
Z-0506-2024 · Root cause: Error in labeling · Recall details · FDA record ↗
Other Stimulator, Nerve, Transcutaneous, For Pain Relief devices
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- Richmar TheraTouch DQ7200Drive Devilbiss Healthcare · Stimulator, Nerve, Transcutaneous, For Pain Relief4 reports
- BiowaveHOME BWHD01Biowave Corporation · Stimulator, Nerve, Transcutaneous, For Pain Relief4 reports
- Belifu TENSHong Qiangxing (Shen Zhen) Electronics Limited · Stimulator, Nerve, Transcutaneous, For Pain Relief3 reports
- Richmar TheraTouch DQ8200Drive Devilbiss Healthcare · Stimulator, Nerve, Transcutaneous, For Pain Relief2 reports
- Roscoe Medical DQ8450Drive Devilbiss Healthcare · Stimulator, Nerve, Transcutaneous, For Pain Relief1 report
- CHATTANOOGA 7560Djo, LLC · STIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF1 report
- Belifu TENSHong Qiangxing (Shen Zhen) Electronics Limited · Stimulator, Nerve, Transcutaneous, For Pain Relief1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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