Carriere 424-917RNRecalls & reported problems
Ortho Organizers, Inc. · Carriere® MOTION 3D COLORS™ Class II 17mm-Silver · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00190707023140), received between Sep 5, 2017 and Sep 5, 2017 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.
InjurySep 5, 2017Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
WHILE THE TECHNICIAN WAS REMOVING CARRIERE MOTION CLASS II 17 MM RIGHT DEVICE, MAXILLARY 1ST BICUSPID FRACTURED. IN ADDITION THE TOOTH FRACTURING, THE PLIERS THAT WERE BEING USED WERE BROKEN DURING THE PROCEDURE.
Patient problems: Tooth Fracture
MAUDE report 6843863 ↗
Other BRACKET, METAL, ORTHODONTIC devices
- Maestro 711-299MCQOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 recall0 reports
- Maestro 711-298QOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 recall0 reports
- Maestro 711-206-10Ortho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 recall0 reports
- Carriere 424-925CNOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC2 reports
- Carriere® SLX 3D™ 777-LR4-HK-10Ortho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
- Carriere 425-425ROrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
- Carriere 424-916CNOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
- Carriere 424-925LNOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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