Midwest T1 Energo 6814680Recalls & reported problems
SIRONA Dental Systems GmbH · Midwest® T1 Energo S 1:5 L · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 14
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI E27668146800), received between Jul 23, 2024 and Apr 23, 2026 — classified as 14 malfunctions.
The most frequently reported specific device problem is “Overheating of Device” (14 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Overheating of Device14
Patient problems
- No Clinical Signs, Symptoms or Conditions14
- Burn(s)3
- Insufficient Information1
Recent adverse event reports
The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 23, 2026Overheating of Device
THIS REPORT SUMMARIZES 8 MALFUNCTION EVENTS WHERE A MIDWEST ENERGO S 1:5 HANDPIECE OVERHEATED. 7 EVENTS RESULTED IN NO INJURY. 1 EVENT RESULTED IN PATIENT BEING SLIGHTLY BURNED WITH NO INTERVENTION.
Patient problems: Burn(s); No Clinical Signs, Symptoms or Conditions
MAUDE report 24964052 ↗MalfunctionJan 20, 2026Overheating of Device
THIS REPORT SUMMARIZES 10 MALFUNCTION EVENTS WHERE MIDWEST ENERGO S 1:5 HANDPIECES OVERHEATED. 10 EVENTS RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24115982 ↗MalfunctionJan 20, 2026Overheating of Device
THIS REPORT SUMMARIZES 11 MALFUNCTION EVENTS WHERE MIDWEST ENERGO 1:5 HANDPIECES OVERHEATED. 7 EVENTS RESULTED IN NO INJURY. 4 EVENTS RESULTED IN THE PATIENT BEING SLIGHTLY BURNED WITH NO INTERVENTION.
Patient problems: Burn(s); No Clinical Signs, Symptoms or Conditions
MAUDE report 24115978 ↗MalfunctionJan 20, 2026Overheating of Device
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT WHERE MIDWEST ENERGO 1:5 HANDPIECE OVERHEATED. 1 EVENT RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24115975 ↗MalfunctionOct 27, 2025Overheating of Device; Overheating of Device
THIS REPORT SUMMARIZES 6 MALFUNCTION EVENTS WHERE MIDWEST ENERGO 1:5 HANDPIECES OVERHEATED. 4 EVENTS RESULTED IN NO INJURY. 2 EVENTS RESULTED IN UNKNOWN INJURY.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 23389477 ↗MalfunctionOct 27, 2025Overheating of Device; Overheating of Device
THIS REPORT SUMMARIZES 17 MALFUNCTION EVENTS WHERE MIDWEST ENERGO S 1:5 HANDPIECES OVERHEATED. 15 EVENTS RESULTED IN NO INJURY. 1 EVENT RESULTED IN THE PATIENT BEING SLIGHTLY BURNED WITH NO INTERVENTION. 1 EVENT RESULTED IN THE PATIENT BEING SLIGHTLY BURNED WITH OINTMENT APPLIED.
Patient problems: Burn(s); No Clinical Signs, Symptoms or Conditions
MAUDE report 23389467 ↗MalfunctionOct 27, 2025Overheating of Device; Overheating of Device
THIS REPORT SUMMARIZES 8 MALFUNCTION EVENTS WHERE MIDWEST ENERGO 1:5 HANDPIECES OVERHEATED. 8 EVENTS RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23389464 ↗MalfunctionOct 27, 2025Overheating of Device; Overheating of Device
THIS REPORT SUMMARIZES 5 MALFUNCTION EVENTS WHERE A MIDWEST ENERGO 1:5 HANDPIECE OVERHEATED. 5 EVENTS RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23389460 ↗MalfunctionJul 22, 2025Overheating of Device; Overheating of Device
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT WHERE A MIDWEST ENERGO 1:5 HANDPIECE OVERHEATED. 1 EVENT RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22564076 ↗MalfunctionJul 22, 2025Overheating of Device; Overheating of Device
THIS REPORT SUMMARIZES 5 MALFUNCTION EVENTS WHERE A MIDWEST ENERGO 1:5 HANDPIECE OVERHEATED. 5 EVENTS RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22564074 ↗MalfunctionJul 22, 2025Overheating of Device; Overheating of Device
THIS REPORT SUMMARIZES 4 MALFUNCTION EVENTS WHERE A MIDWEST ENERGO S 1:5 HANDPIECE OVERHEATED. 4 EVENTS RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22564015 ↗MalfunctionApr 22, 2025Overheating of Device; Overheating of Device
THIS REPORT SUMMARIZES 3 MALFUNCTION EVENTS WHERE A MIDWEST ENERGO 1:5 HANDPIECE OVERHEATED. 3 EVENTS RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21880821 ↗MalfunctionJan 24, 2025Overheating of Device; Overheating of Device
THIS REPORT SUMMARIZES 7 MALFUNCTION EVENTS WHERE A MIDWEST ENERGO S 1:5 HANDPIECE OVERHEATED. 7 EVENTS RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21232213 ↗MalfunctionJul 23, 2024Overheating of Device; Overheating of Device
THIS REPORT SUMMARIZES 3 MALFUNCTION EVENTS WHERE A MIDWEST ENERGO 1:5 HANDPIECE OVERHEATED. 3 EVENTS RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19805658 ↗
Other Handpiece, air-powered, dental devices
- Henry Schein Maxima 5702660Henry Schein, Inc. · Handpiece, air-powered, dental15 reports
- Midwest® E Plus 875205SIRONA Dental Systems GmbH · Handpiece, Air-Powered, Dental12 reports
- HENRY SCHEIN 5701072Henry Schein, Inc. · Handpiece, air-powered, dental11 reports
- Midwest® E mini 875101SIRONA Dental Systems GmbH · Handpiece, Air-Powered, Dental10 reports
- Midwest® E Pro 875105SIRONA Dental Systems GmbH · Handpiece, Air-Powered, Dental10 reports
- Maxima 5702094Henry Schein, Inc. · Handpiece, air-powered, dental8 reports
- Midwest Tradition® 790344SIRONA Dental Systems GmbH · Handpiece, Air-Powered, Dental5 reports
- Z890LNakanishi Inc. · Handpiece, air-powered, dental5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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