TriLeap Lower Extremity Anatomic Plating System 2.5 mm Ti Variable Angle Screw Length 34 mm, MagentaRecalls & reported problems
Crossroads Extremity Systems · 2.5 mm Ti Variable Angle Screw Length 34 mm, Magenta · Class 2 · Implant
All models of TriLeap Lower Extremity Anatomic Plating System (57)
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 00810112593570), received between Oct 23, 2024 and Oct 23, 2024 — classified as 1 malfunction.
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
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 23, 2024Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED ON (B)(6) 2024, THE SURGEON WAS USING THE TRILEAP CUBOID LOCKING PLATE FOR A COMMINUTED CUBOID FRACTURE. HE DETERMINED LOCKING SCREWS WOULD BE THE ONLY SCREWS NECESSARY TO USE AFTER REDUCING THE FRACTURE. 6 OUT OF THE 7 LOCKING SCREWS DID NOT EFFECTIVELY LOCK INTO THE PLATE. SCREWS WERE LEFT IN. PATIENT WILL BE NON-WEIGHT BEARING FOR A WHILE DUE TO ADDITIONAL POLY TRAUMA INJURIES. THERE WAS NO SURGERY DELAYED DUE TO THE REPORTED EVENT.
Patient problems: Insufficient Information
MAUDE report 20514578 ↗
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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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