DYONICS ELECTROBLADE BONECUTTER 72202213Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00885554015348), received between Mar 5, 2021 and Apr 9, 2021 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Break” (2 reports).

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 9, 2021Failure to Deliver Energy; Failure to Deliver Energy

  IT WAS REPORTED THAT, DURING AN ARTHROSCOPY, THE ELECTROBLADE DID NOT GET AN ENERGY OUTPUT WHEN USING A COAGULATION. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH A SMITH AND NEPHEW BACK-UP DEVICE. NO PATIENT INJURIES, DELAYS 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 11640399 ↗
• InjuryMar 5, 2021Break; Break

  IT WAS REPORTED THAT DURING A SURGERY, THE ELECTROBLADE RESECTOR OUTSIDE SHEATH WAS LOOSE AND CAME APART. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITHOUT A SIGNIFICANT DELAY USING A BACK UP DEVICE. NO 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 11420748 ↗
• InjuryMar 5, 2021Break; Break

  IT WAS REPORTED THAT DURING A SURGERY, THE ELECTROBLADE RESECTOR OUTSIDE SHEATH WAS LOOSE AND CAME APART. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITHOUT A SIGNIFICANT DELAY USING A BACK UP DEVICE. NO 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 11420745 ↗