MotoBAND™ CP DynaForce® DynaBunion Plate 18mm Right Single PackRecalls & reported problems
Crossroads Extremity Systems · The MotoBAND™ CP DynaForce® Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00815432028870), received between Dec 8, 2021 and Sep 29, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Migration” (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
- Appropriate Device Problem Term/Code Not Available1
- Migration1
Patient problems
- Implant Pain1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2022Migration; Migration
AT ROUTINE FOLLOW-UP, THE SURGEON IDENTIFIED THE ANTI-DRIFT BOLT WAS THROUGH THE PLATE AT 2 WEEKS POST-OP. AT 6 WEEKS POST-OP, THE SURGEON NOTES THAT THE IM ANGLE IS INCREASED. THE PATIENT IS ASYMPTOMATIC, AND NO REVISION IS PLANNED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15501543 ↗MalfunctionDec 8, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
THE SURGEON SUBMITTED A CASE SERIES OF DYNABUNION SYSTEM. THE ANTI-DRIFT BLOT HAS BACKED OUT AS SHOWN IN THE 6-WEEK X-RAY. THE SCREW HEAD PROMINENT ABOVE THE PLATE. THE PATIENT WAS ASYMPTOMATIC AND REVISION SURGERY WAS NOT SCHEDULED AT THE TIME OF THE REPORT. THE SURGEON REPORTED AT A LATER DATE THAT THE SYSTEM WAS REMOVED AFTER A PERIOD OF NON-WEIGHT BEARING. THE PATIENT STATUS AFTER THE REVISION IS UNKNOWN.
Patient problems: Implant Pain
MAUDE report 12964836 ↗
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- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
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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