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Carriere 424-916CNRecalls & reported problems

Ortho Organizers, Inc. · Carriere® MOTION 3D COLORS™ Class II 16mm-Silver · 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 00190707023096), received between Dec 29, 2021 and Dec 29, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1

Patient problems

  • Tooth Fracture1

Recent adverse event reports

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

  • InjuryDec 29, 2021Insufficient Device Problem Information; Insufficient Device Problem Information

    UPON DEBONDING OF A CARRIERE MOTION 3D COLOR CLASS II 16 MM (SILVER) DEVICE BY THE DOCTOR'S ASSISTANT, THE (B)(6) FEMALE PATIENT EXPERIENCED SHEARING OF THE FACIAL SURFACES OF BOTH UPPER CANINE TEETH (TEETH # 6 AND 11). ACCORDING TO THE DOCTOR'S COMPLAINT, THE 3D MOTION DEVICE HAD BEEN ATTACHED TO THE ETCHED CANINES WITH TRANSBOND ADHESIVE BOND MATERIAL.

    Patient problems: Tooth Fracture

    MAUDE report 13113070 ↗

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