T2 1825-1040SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04546540199539), received between Aug 15, 2016 and May 10, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 10, 2019Improper or Incorrect Procedure or Method

  CUSTOMER REPORTED THAT SURGEON PERFORMED A RETROGRADE FEMORAL NAIL ON (B)(6) 2019 ON A PERI-PROSTHETIC FRACTURE. THE ATTENDING THEATRE NURSE INFORMED (B)(4) THAT SHE HAD FILED A REPORT AS THE IMPLANT THAT WAS USED HAD AN EXPIRY ON 01/19. SURGEON WAS MADE AWARE OF THIS BEFORE IMPLANTING BUT WAS HAPPY TO PROCEED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8601756 ↗
• MalfunctionAug 15, 2016Break; Fracture; Fracture

  IT HAS BEEN REPORTED THAT A T2 NAIL HAS BROKEN DURING SURGERY.

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

  MAUDE report 5876680 ↗