T2 2339-1140SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327293746), received between Feb 21, 2022 and Jul 20, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (2 reports).

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.

• InjuryJul 20, 2023Break; Fracture; Break; Fracture

  AS REPORTED: "PATIENT CAME IN AROUND 7 MONTHS AFTER FIRST SURGERY AND THE NAIL BROKE RIGHT AT THE 6TH MOST DISTAL STATIC HOLE. THIS LED TO A NON-UNION AND REVISION SURGERY TO REPLACE THE BROKEN NAIL."

  Patient problems: Failure of Implant; Nonunion/Delayed-union Bone Fracture

  MAUDE report 17366639 ↗
• InjuryFeb 21, 2022Break; Fracture; Break; Fracture

  THE PATIENT FELT A "SNAP" WHILE WALKING. X-RAYS SHOWED A BROKEN NAIL. REVISION SURGERY WAS USED TO REMOVE NAIL, AND REPLACED WITH A T2 SUPRACONDYLAR NAIL AND A DISTAL LATERAL FEMUR PLATE.

  Patient problems: Failure of Implant

  MAUDE report 13573133 ↗