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DYONICS 72204127Recalls & reported problems

Smith & Nephew, Inc. · DYONICS WIRE DRVR SM BAT HANDPIECE · Class 1

All models of DYONICS (22)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885554033588), received between May 14, 2018 and May 14, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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

Device problems

  • Device Operates Differently Than Expected1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 14, 2018Device Operates Differently Than Expected

    IT WAS REPORTED THAT THE DEVICE PRESENTED A FALSE CHANNEL. NO PATIENT INJURY REPORTED. THERE WAS NOT BACKUP AVAILABLE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7512220 ↗

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Sources and updates

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