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NA 72201500SRecalls & reported problems

Smith & Nephew, Inc. · DYONICS POWERMINI SHAVER, HAND-CONTROLLED, SERVICE REPLACEMENT · Class 1

Adverse event reports
5
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 03596010654823), received between Sep 10, 2020 and Apr 25, 2025 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 1 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Overheating of Device2
  • Connection Problem1
  • Physical Resistance/Sticking1
  • Protective Measures Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions3
  • No Patient Involvement2

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 25, 2025Physical Resistance/Sticking; Physical Resistance/Sticking

    UPON INVESTIGATION IT WAS DETERMINED THAT THE DYONICS POWERMINI SHAVER'S BUTTON WAS STUCK CAUSING THE SHAVER TO RUN CONTINUOUSLY. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21914047 ↗
  • MalfunctionApr 25, 2022Overheating of Device; Overheating of Device

    IT WAS REPORTED THAT THE DYONICS POWERMINI GEARBOX CLICKS, JAMS AND OVERHEATS. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14198016 ↗
  • MalfunctionAug 30, 2021Overheating of Device; Overheating of Device

    IT WAS REPORTED THAT THE GEARBOX OF THE DYONICS POWER OVERHEATS. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12388470 ↗
  • MalfunctionNov 19, 2020Protective Measures Problem; Protective Measures Problem

    IT WAS REPORTED THAT THE DYONICS POWERMINI DISPLAYED "UNKNOWN HANDPIECE" ERROR MESSAGE. NO CASE INVOLVED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

    Patient problems: No Patient Involvement

    MAUDE report 10871484 ↗
  • MalfunctionSep 10, 2020Connection Problem; Connection Problem

    IT WAS REPORTED THAT THE DYONICS POWER MINI DID NOT RECOGNIZE THE CONTROL UNIT. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

    Patient problems: No Patient Involvement

    MAUDE report 10515710 ↗

Other SAW, POWERED, AND ACCESSORIES devices

All SAW, POWERED, AND ACCESSORIES devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.