MotoBAND™ CP DynaForce® DynaBunion Plate 18mm Left 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
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00815432028788), received between May 23, 2022 and Jan 17, 2025 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Appropriate Device Problem Term/Code Not Available1
- Break1
Patient problems
- Hypersensitivity/Allergic reaction1
- Implant Pain1
- Pain1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJan 17, 2025Break; Break
IT WAS REPORTED THAT THE USER'S HARDWARE BROKE WITHIN A COUPLE MONTHS OF BEING PLACED. THE USER REQUIRED A SECOND SURGERY TO REMOVE THE HARDWARE. PIECES OF HARDWARE WERE LEFT IN THE USER'S FOOT.
Patient problems: Pain
MAUDE report 21178067 ↗InjuryDec 27, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT ON AN UNKNOWN DATE, A PATIENT THOUGHT THAT SHE MIGHT BE HAVING AN ALLERGIC REACTION TO A PLATE AFTER HER SURGERY. SHE HAD A CROSSROADS EXTREMITY SYSTEMS PLATE IMPLANTED APPROXIMATELY 14 WEEKS PRIOR TO ON (B)(6) 2022. THE IMPLANTS WILL NOT BE RECOVERED. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT INVOLVES ONE THE MOTOBAND¿ CP DYNAFORCE® IMPLANT SYSTEM IS A BONE PLATING SYSTEM. THIS IS REPORT 2 OF 2 FOR (B)(4).
Patient problems: Hypersensitivity/Allergic reaction
MAUDE report 16053024 ↗MalfunctionMay 23, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ON (B)(6), 2022, THE SURGEON REMOVED DYNABUNION IMPLANTS THAT WERE IMPLANTED (B)(6), 2021. IMPLANTS WERE REMOVED PER PATIENT REQUEST DUE TO PROMINENCE LEADING TO IRRITATION. HARDWARE WAS REMOVED AND NOT REPLACED. UNION WAS PRESENT.
Patient problems: Implant Pain
MAUDE report 14478311 ↗
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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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