TriLEAP 1st MTP Ti Fusion Plate, Extra Small, 5 Hole, 0 Deg, RightRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810112599176), received between Mar 5, 2026 and Mar 5, 2026 — 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.

Most reported problems

Recent adverse event reports

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

• MalfunctionMar 5, 2026Device-Device Incompatibility

  IT WAS REPORTED THAT THE 1ST MTP TI PL XS 5H 0 DEG RT TRILEAP(TM) EXPERIENCED A FAILURE WHERE LOCKING GUIDES WOULD NOT LOCK INTO THE PLATE, ALTHOUGH THE GUIDE WOULD LOCK INTO ANOTHER PLATE. THE EVENT OCCURRED DURING THE PRE-OPERATIVE PHASE. THERE WAS NO PATIENT INVOLVEMENT OR CONSEQUENCE AS THE ISSUE WAS IDENTIFIED BEFORE USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24519872 ↗