DYONICS POWER 7209392Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010466204), received between May 5, 2021 and May 5, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Noise, Audible” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMay 5, 2021No Apparent Adverse Event; Noise, Audible; No Apparent Adverse Event; Noise, Audible

  IT WAS REPORTED THAT DURING AN ARTHROSCOPIC LATARJET THE DYONICS'S MOTOR SOUNDED OFF AND STOPPED WORKING MIDWAY THROUGH SAWING THE CORACOID. THE PROCEDURE WAS SUCCESSFULLY COMPLETED BY MANUALLY USING THE SAW BLADE. A CHANGE OF TECHNIQUE WAS USED WITHOUT DELAY. 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 11781009 ↗