T2 1818-1020SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540673282), received between Apr 7, 2026 and Apr 7, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Malposition of Device” (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.

• MalfunctionApr 7, 2026Positioning Failure; Malposition of Device

  AS REPORTED: "DURING SURGERY TO INSERT A T2 ANKLE NAIL, A 4.2 MM DRILL BIT BROKE AT BOTH THE PROXIMAL AND DISTAL FIXATION SCREW INSERTION SITES AFTER COMING INTO CONTACT WITH THE NAIL. THIS RESULTED IN THE BREAKAGE OF TWO DRILL BITS. AS THE HOSPITAL HAD A GMMA4 FIXATION DRILL OF THE SAME DIAMETER IN STOCK, THIS WAS USED AS A SUBSTITUTE TO COMPLETE THE OPERATION.".

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 24807298 ↗