Roscoe Medical DT7202 / DT7202CARecalls & reported problems
Drive Devilbiss Healthcare · T7 Massage Digital (DT7202CA) · Class 2
All models of Roscoe Medical (4)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00092237616796), received between Feb 27, 2026 and Feb 27, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
Patient problems
- Electric Shock1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 27, 2026Insufficient Device Problem Information
AFFECTED PRODUCTS: B00NCRE4GO - TENS 7000 DIGITAL TENS UNIT WITH ACCESSORIES - TENS UNIT MUSCLE STIMULATOR FOR BACK PAIN. RELIEF, SHOULDER PAIN RELIEF, NECK PAIN, SCIATICA PAIN RELIEF, NERVE PAIN RELIEF ASIN VARIATIONS: NA. CUSTOMER FEEDBACK: (B)(6) 2024: "DOES NOT STIMULATE. SHOCKS. CAUSED ME TO GO INTO CARDIAC ARREST."
Patient problems: Electric Shock
MAUDE report 24468313 ↗
Other Stimulator, Nerve, Transcutaneous, Over-The-Counter devices
- Aleve 1613538Bayer Healthcare LLC · Stimulator, Nerve, Transcutaneous, Over-The-Counter4 reports
- Enso M3Hinge Health, Inc. · Stimulator, Nerve, Transcutaneous, Over-The-Counter2 reports
- WiTouch 11.1510Hollywog, LLC · Stimulator, Nerve, Transcutaneous, Over-The-Counter2 reports
- AUVON AS8012-041Shenzhen Yuwen E-Commerce Co., Ltd. · Stimulator, Nerve, Transcutaneous, Over-The-Counter1 report
- WiTouch Pro 11.1500Hollywog, LLC · Stimulator, Nerve, Transcutaneous, Over-The-Counter1 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.
How reports and recalls are matched · Editorial policy · Report an error on this page