MEDIDENTA TT1200Recalls & reported problems
Handpiece Parts & Repairs, Inc. · MEDIDENTA TURBO TORQUE 1200 MINI HEAD · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00810988030445), received between Aug 27, 2024 and Feb 11, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. 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
- Detachment of Device or Device Component2
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 11, 2026Detachment of Device or Device Component
DURING USE, THE HEAD ASSEMBLY SEPARATED FROM THE HANDPIECE WHILE IN PATIENT'S MOUTH.
Patient problems: Insufficient Information
MAUDE report 24319031 ↗MalfunctionAug 27, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
HANDPIECES FELL APART DURING USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20082367 ↗
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