DeRoyal 89-4712Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00749756604925), received between Apr 9, 2026 and Apr 27, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Activation, Positioning or Separation 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 27, 2026Activation, Positioning or Separation Problem

  A USER FACILITY REPORTED, "BOVIE WOULD NOT WORK."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25003047 ↗
• MalfunctionApr 9, 2026

  BOVIE WOULD NOT WORK.

  Patient problems: Insufficient Information

  MAUDE report 24828280 ↗