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Triumph® 205-202Recalls & reported problems

Ortho Organizers, Inc. · Triumph® Weingart Pliers · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00190707081621), received between Oct 16, 2020 and Oct 16, 2020 — classified as 1 injury.

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

Most reported problems

Device problems

  • Break1

Patient problems

  • Abrasion1

Recent adverse event reports

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

  • InjuryOct 16, 2020Break; Break

    THE TIP OF THE TRIUMPH WEINGART PLIER BROKE OFF WHILE BEING USED IN THE MOUTH DURING ORTHODONTIC TREATMENT RESULTING IN INJURY TO THE INNER CHEEK. THE BROKEN PIECE WAS RETRIEVED WITHOUT FURTHER INCIDENT. PATIENT WAS PRESCRIBED PAINKILLERS AND ANTIBIOTICS TO TREAT THE INNER CHEEK INJURY.

    Patient problems: Abrasion

    MAUDE report 10693788 ↗

Other PLIER, ORTHODONTIC devices

All PLIER, ORTHODONTIC devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.