T2 Boost 6689629Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI E27666896290), received between Oct 27, 2025 and Oct 27, 2025 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 27, 2025Overheating of Device; Overheating of Device

  THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT WHERE A T2 BOOST S HANDPIECE OVERHEATED. 1 EVENT RESULTED IN THE PATIENT BEING SLIGHTLY BURNED WITH NO INTERVENTION.

  Patient problems: Burn(s)

  MAUDE report 23389480 ↗