MotoBAND™ CP DynaForce® DynaForce Plate Sterile Instrument KitRecalls & 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. When used for these indications, certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00815432027187), received between Mar 6, 2020 and Jan 22, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Material Deformation2
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Insufficient Information2
- No Code Available1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 22, 2024Material Deformation; Material Deformation
IT WAS REPORTED THAT ON UNKNOWN DATE, THE OLIVE WIRES IN THE PLATE INSTRUMENT KIT WERE BENT WHEN THE SCRUB TECH OPENED IT. THIS WAS DISCOVERED PRE-OPERATIVELY WITH NO PATIENT INVOLVEMENT. THIS REPORT IS FOR ONE DYNAFORCE PL INSTR KIT STERILE FOR (B)(4).
Patient problems: Insufficient Information
MAUDE report 18557871 ↗MalfunctionJan 22, 2024Material Deformation; Material Deformation
IT WAS REPORTED THAT ON UNKNOWN DATE, THE OLIVE WIRES IN THE PLATE INSTRUMENT KIT WERE BENT WHEN THE SCRUB TECH OPENED IT. THIS WAS DISCOVERED PRE-OPERATIVELY WITH NO PATIENT INVOLVMENT. THIS REPORT IS FOR ONE DYNAFORCE PL INSTR KIT STERILE FOR (B)(4).
Patient problems: Insufficient Information
MAUDE report 18557814 ↗MalfunctionMar 6, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
AN MTP SURGERY WAS PERFORMED ON (B)(6) 2020. THE UNI-AXIAL SCREW WOULD NOT SEAT FULLY. THE SURGEON ATTEMPTED TO REMOVE WITH AN H-10 G-SOURCE DRIVER AND PULLED THE SCREW FROM THE HOLE. THE SURGEON PLACED A 3.0 NON-LOCKING SCREW AND COMMENTED THAT THE SCREW DID NOT BIT INTO THE BONE.
Patient problems: No Code Available
MAUDE report 9801771 ↗
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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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