Carriere 424-926RNRecalls & reported problems
Ortho Organizers, Inc. · Carriere® MOTION 3D COLORS™ Class II 26mm-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 00190707023416), received between Oct 16, 2020 and Oct 16, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Separation Failure” (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
- Separation Failure1
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 16, 2020Separation Failure; Separation Failure
DOCTOR WAS REMOVING THE CARRIERE MOTION ORTHODONTIC APPLIANCE FROM THE PATIENT'S TOOTH AND THE INCISAL 1/3 OF THE CROWN BROKE OFF. NO PULP EXPOSURE BUT SHE WAS EXTREMELY SENSITIVE AND WILL NEED A CROWN. DOCTOR REMOVED THE APPLIANCE USING PIN AND LIGATURE CUTTERS AS THE PATIENT WAS BITING INTO A COTTON ROLL. SHE APPLIED PRESSURE FROM THE GINGIVAL AND OCCLUSAL, AND DID NOT TORQUE THE TOOTH. COMPLAINT RECEIVED BY ORTHO ORGANIZERS, INC. ON (B)(6) 2020.
Patient problems: Tooth Fracture
MAUDE report 10693786 ↗
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 424-917RNOrtho 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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