Skip to content

TriMAX Implant System TriMAX 18mm Full Prep KitRecalls & reported problems

Crossroads Extremity Systems · The TriMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00815432027590), received between Sep 29, 2022 and Sep 29, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1
  • Migration1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 29, 2022Fracture; Migration; Fracture; Migration

    THE SURGEON PERFORMED AN ISOLATED TN FUSION ON (B)(6) 2020. THE PATIENT WAS FUSED, AND DEVICES WERE INTACT AT 60 DAYS POST-OP. AT 85 DAYS POST-OP, THE X-RAY REVEALS THAT THE KEEL ON THE KEEL-LOCK STAPLE HAS BROKEN AND THE STAPLE HAS BACKED OUT OF THE BONE. THE PATIENT WAS WEIGHT-BEARING IN A CAM BOOT 1 WEEK PRIOR TO OBSERVATION OF THE BROKEN STAPLE. FUSION REMAINS INTACT DESPITE THE BACK-OUT OF THE STAPLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15501549 ↗

Other Staple, Fixation, Bone devices

All Staple, Fixation, Bone devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page