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
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 ↗
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- NA 72201500Smith & Nephew, Inc. · SAW, POWERED, AND ACCESSORIES136 reports
- PLATINUM 72205321Smith & Nephew, Inc. · SAW, POWERED, AND ACCESSORIES118 reports
- Zimmer Biomet™ 89-8509-450-60Zimmer Surgical SA · Saw, Powered, And Accessories83 reports
- NA 72200617Smith & Nephew, Inc. · SAW, POWERED, AND ACCESSORIES77 reports
- NA 72202530Smith & Nephew, Inc. · SAW, POWERED, AND ACCESSORIES53 reports
- DYONICS INCISOR 72203013Smith & Nephew, Inc. · SAW, POWERED, AND ACCESSORIES46 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.