Midwest® E mini 875181Recalls & reported problems
SIRONA Dental Systems GmbH · Midwest® E mini PL 1:5 · Class 1
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 E2768751810), received between Apr 23, 2026 and Apr 23, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Overheating of Device” (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.
Reports received per month
Most reported problems
Device problems
- Overheating of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 23, 2026Overheating of Device
THIS REPORT SUMMARIZES 15 MALFUNCTION EVENTS WHERE MIDWEST E PRO 1:5 HIGH SPEED CONTRA ANGLE ATTACHMENT HANDPIECES OVERHEATED. 15 EVENTS RESULTED IN NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24964087 ↗
Other Handpiece, Air-Powered, Dental devices
- Henry Schein Maxima 5702660Henry Schein, Inc. · Handpiece, air-powered, dental15 reports
- Midwest T1 Energo 6814680SIRONA Dental Systems GmbH · Handpiece, air-powered, dental14 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
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page