Home › Drive Devilbiss Healthcare › Richmar TheraTouch
Richmar TheraTouch
Drive Devilbiss Healthcare · Model DQSWD2 · UDI-DI 00092237620397
IMJ
Prescription
10
510(k) clearances
25
Adverse events
1
Recalls
16
Facilities
Description
DX2 Shortwave Diathermy Clinical Device
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-08-21 | DJO, LLC | Overheating and burning of the wire insulation inside the applicator. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.