MiniBunion™ MiniBunion Plate, 4.5mm Offset, Long - SterileRecalls & reported problems
Crossroads Extremity Systems · The MiniBunion™ Implant System is indicated for stabilization and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of an intramedullary implant and screws. · Class 2 · Implant
All models of MiniBunion (7)
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 00815432027170), received between Apr 29, 2021 and Sep 8, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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
- Device-Device Incompatibility1
- Fracture1
Patient problems
- Malunion of Bone1
- 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 8, 2025Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT DURING INSPECTION; THE DEVICE WOULDN'T THREAD. NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22994980 ↗MalfunctionApr 29, 2021Fracture; Fracture
THE ORIGINAL BUNION CORRECTION WAS PERFORMED ON (B)(6) 2019 WITH THE CROSSROADS MINIBUNION PRODUCTS LISTED ABOVE. X-RAY EVIDENCE IMMEDIATELY POST-OPERATION SHOWS THE PLATE NOT FULLY SEATED ONTO THE SHAFT OF THE 1ST METATARSAL AND A GAP AT THE OSTEOTOMY SITE. AT A 1-YEAR POST-OP FOLLOW UP VISIT, X-RAY EVIDENCE SHOWS A NON-UNION OF THE OSTEOTOMY AND A BROKEN NON-LOCKING SCREW .THE PATIENT IS VITAMIN D DEFICIENT. A REVISION SURGERY WAS PERFORMED ON (B)(6) 2020 TO ADDRESS THE NON-UNION AND REMOVE ALL HARDWARE. NONE OF THE REPLACEMENT HARDWARE USED WERE CROSSROADS PRODUCTS.
Patient problems: Malunion of Bone
MAUDE report 11747279 ↗
Other Plate, Fixation, Bone devices
- Lapiplasty System 2 SK14Treace Medical Concepts, Inc. · Plate, Fixation, Bone260 reports
- PRECICE® Plating System LP4.5-PRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls6 reports
- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page