Richmar TheraTouch DQ8200Recalls & reported problems
Drive Devilbiss Healthcare · CX4 Combination E-stim/ Ultrasound Clinical Device (4-channel) · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00092237621462), received between Aug 31, 2026 and Sep 24, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Electrical /Electronic Property Problem1
Patient problems
- Burn(s)1
- Deformity/ Disfigurement1
- Full thickness (Third Degree) Burn1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 24, 2026Adverse Event Without Identified Device or Use Problem
Drive Medical was notified of an incident involving an electrotherapy device by an attorney letter who reported that during a physical therapy session, a malfunction of the device caused a third-degree burn to the end user's skin on her right leg and permanent disfigurement to her body. As part of its complaint review and evaluation process, Drive Medical will also notify the manufacturer of the product about this complaint.
Patient problems: Burn(s)
MAUDE report 50880442 ↗InjuryAug 31, 2026Electrical /Electronic Property Problem
Drive Medical was notified of an incident involving an electrotherapy device by an attorney letter who reported that during a physical therapy session, a malfunction of the device caused a third-degree burn to the end user's skin on her right leg and permanent disfigurement to her body. As part of its complaint review and evaluation process, Drive Medical will also notify the manufacturer of the product about this complaint.
Patient problems: Deformity/ Disfigurement; Full thickness (Third Degree) Burn
MAUDE report 50515584 ↗
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
- 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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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