Maestro 711-298QRecalls & reported problems
Ortho Organizers, Inc. · Maestro® .018 Kit U/L 5x5 Roth HK · Class 1
All models of Maestro (3)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
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 16, 2026.
Recalls naming this device
- Apr 2, 2019Terminated
Orthodontic Bracket is mislabeled
Z-2478-2020 · Root cause: Process control · Recall details · FDA record ↗
Other BRACKET, METAL, ORTHODONTIC devices
- Maestro 711-299MCQOrtho 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 424-926RNOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
- Carriere® SLX 3D™ 777-LR4-HK-10Ortho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
- Carriere 424-927RNOrtho Organizers, Inc. · BRACKET, METAL, ORTHODONTIC1 report
- Carriere 424-917RNOrtho 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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