ForceTriad FTBRKITRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521035379), received between Sep 27, 2023 and Sep 27, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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.

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.

• MalfunctionSep 27, 2023Break; Failure to Cut; Adverse Event Without Identified Device or Use Problem; Break; Failure to Cut; Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE REPORTER, DURING PROCEDURE, THE UNIT HAD A FAILURE PROMPT AND THE DEVICE ELECTRO-KNIFE FUNCTION CANNOT BE USED. SUSPECTED OF EQUIPMENT SWITCHBOARD DAMAGE. THERE WAS NO MEDICAL/SURGICAL INTERVENTION OR REOPERATION DONE TO PATIENT. PATIENT WAS NOT ALSO ON ANY MEDICATION. THERE WAS AN UNKNOWN PATIENT HARM.

  Patient problems: Insufficient Information

  MAUDE report 17825803 ↗