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Carriere 424-925LNRecalls & reported problems

Ortho Organizers, Inc. · Carriere® MOTION 3D COLORS™ Class II 25mm-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 00190707023379), received between Oct 26, 2018 and Oct 26, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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

  • Improper or Incorrect Procedure or Method1

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.

  • InjuryOct 26, 2018Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

    WHILE THE TECHNICIAN WAS REMOVING CARRIERE MOTION 3D COLORS CLASS II 25MM LEFT - SILVER, UPPER LEFT 3 CANINE FRACTURED. PER THE DENTIST, THE FOLLOWING STEPS WERE TAKEN: REMOVAL OF EXCESS ADHESIVE WITH HIGH SPEED HAND PIECE; HAVING PATIENT BITE ON COTTON ROLL; SQUEEZING ON EACH SIDE OF PAD WITH BRACKET REMOVING PLIER. DEVICE WAS BONDED ON (B)(6) 2018 AND WAS BEING DEBONDED DUE TO THE PATIENT BEING FINISHED WITH THE TREATMENT STEP.

    Patient problems: Tooth Fracture

    MAUDE report 8009692 ↗

Other BRACKET, METAL, ORTHODONTIC devices

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