Roscoe Medical DQ8450Recalls & reported problems
Drive Devilbiss Healthcare · Quattro 2.5 · 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 00092237611623), received between Sep 24, 2026 and Sep 24, 2026 — classified as 1 injury.
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
Patient problems
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 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 the device provider who reported that during use,the end user received two burns requiring wound care treatment. 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 50880443 ↗
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- Richmar TheraTouch DQ8200Drive Devilbiss Healthcare · Stimulator, Nerve, Transcutaneous, For Pain Relief2 reports
- CHATTANOOGA 7560Djo, LLC · STIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF1 report
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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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