DYONICS 7205841Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 03596010406200), received between Feb 8, 2019 and Mar 20, 2023 — classified as 2 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Display or Visual Feedback 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 16, 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.

• MalfunctionMar 20, 2023Smoking; Unexpected Shutdown; Smoking; Unexpected Shutdown

  IT WAS REPORTED THAT, DURING AN UNSPECIFIED PROCEDURE, WHILE USING THE DYONICS POWER CONTROL UNIT SMOKE CAME OUT AND IT TURNED OFF. IT IS UNKNOWN HOW THE PROCEDURE WAS COMPLETED; HOWEVER, NO SURGICAL DELAY WAS REPORTED. NO FURTHER COMPLICATIONS WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16578553 ↗
• InjuryMar 1, 2022Display or Visual Feedback Problem; Electrical Shorting; No Apparent Adverse Event; Display or Visual Feedback Problem; Electrical Shorting; No Apparent Adverse Event

  IT WAS REPORTED THAT, DURING AN ARTHROSCOPY, THE DYONICS POWER CONTROL UNIT DID NOT WORK AND DID NOT LIGHT UP. ADDITIONALLY, THE FOOTPEDAL DID NOT WORK EITHER WHEN CONNECTED TO IT. THE PROCEDURE WAS COMPLETED WITH A SIGNIFICANT DELAY (40 MINUTES) USING AN UNKNOWN COMPETITOR DEVICE. NO OTHER COMPLICATIONS WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13636449 ↗
• InjuryJan 7, 2021No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT DURING A SURGERY THE CONTROL UNIT WAS DEFECTIVE. THE PROCEDURE WAS COMPLETED WITHOUT A SIGNIFICANT DELAY. A COMPETITOR DEVICE WAS USED. NO PATIENT INJURY OR OTHER COMPLICATIONS WERE REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11130810 ↗
• MalfunctionFeb 8, 2019Electrical /Electronic Property Problem

  IT WAS REPORTED THAT THE POWER BOARD HAS BLOW RENDERING THE MACHINE INOPERABLE. NO BACKUP DEVICE WAS AVAILABLE; THEREFORE, THE PROCEDURE WAS NOT COMPLETED AS INTENDED. THERE WAS A SURGICAL DELAY GREATER THAN 30 MINUTES; NO PATIENT INJURIES OR COMPLICATIONS WERE REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8322901 ↗