MEDIDENTA TT2200Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00810988030902), received between May 5, 2026 and Jun 18, 2026 — classified as 2 injuries.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 18, 2026Detachment of Device or Device Component

  HEAD CAP DISLODGED FROM THE HANDPIECE DURING USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25553240 ↗
• InjuryMay 5, 2026Detachment of Device or Device Component

  HEAD CAP DISLODGED FROM THE HANDPIECE DURING USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25086238 ↗