DYONICS POWER 7205785Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 03596010410702), received between Jan 30, 2018 and Aug 8, 2018 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Circuit Failure” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 8, 2018Electrical Shorting

  IT WAS REPORTED THAT DEVICE HAD A SHORT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7763580 ↗
• MalfunctionMar 26, 2018Circuit Failure

  IT WAS REPORTED THAT THE DEVICE SHORTED. NO DELAY OR PATIENT INJURES WERE REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7369755 ↗
• MalfunctionFeb 20, 2018Failure to Shut Off

  IT WAS REPORTED THAT WHEN TRIGGER IS RELEASED THE HANDPIECE CONTINUES TO RUN. NO PATIENT INJURY WAS REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7281561 ↗
• MalfunctionJan 30, 2018Electrical /Electronic Property Problem

  IT WAS REPORTED THAT THE DEVICE HAD A SHORT. NO PATIENT INJURY REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7228237 ↗