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Carriere 424-925CNRecalls & reported problems

Ortho Organizers, Inc. · Carriere® MOTION 3D COLORS™ Class II 25mm-Silver · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00190707023362), received between May 30, 2017 and May 30, 2017 — classified as 2 injuries.

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

  • Adverse Event Without Identified Device or Use Problem2

Patient problems

  • Tooth Fracture2

Recent adverse event reports

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

  • InjuryMay 30, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    WHEN REMOVING THE CARRIERE MOTION APPLIANCE FROM TOOTH NUMBER 14, A SMALL FRACTURE OF ENAMEL BROKE OFF WITH THE APPLIANCE LOCATED ON THE BUCCAL SIDE.

    Patient problems: Tooth Fracture

    MAUDE report 6599793 ↗
  • InjuryMay 30, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    TOOTH FRACTURE WHILE DEBONDING CARRIERE MOTION APPLIANCE WHEN REMOVING THE CARRIERE FROM #11 TOOTH, THE MESIAL EDGE OF THE TOOTH FRACTURED OFF WITH THE CARRIERE. THE PATIENT IS SYMPTOM FREE.

    Patient problems: Tooth Fracture

    MAUDE report 6599788 ↗

Other BRACKET, METAL, ORTHODONTIC devices

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Sources and updates

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