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SegWAY ECTR-d T400-023Recalls & reported problems

Trice Medical, Inc. · Endoscopic Carpal Tunnel Release, 2.3mm, Complete Set · Class 1

Data updated Oct 18, 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 00857356008156), received between Mar 9, 2023 and Mar 9, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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 18, 2026.

Most reported problems

Device problems

  • Contamination /Decontamination Problem1

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.

  • MalfunctionMar 9, 2023Contamination /Decontamination Problem; Contamination /Decontamination Problem

    A USER REPORTED THAT THERE WAS A RED DEPOSIT ON THE SIDE OF A PAIR OF SCISSORS INSIDE THE DISPOSABLE KIT OF INSTRUMENTS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16519210 ↗

Other Kit, Surgical Instrument, Disposable devices

All Kit, Surgical Instrument, Disposable devices →

Sources and updates

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