T2 ALPHA 2333-1144SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327286595), received between Jan 23, 2023 and Jan 23, 2023 — classified as 1 injury.

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 16, 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.

• InjuryJan 23, 2023Break; Fracture; Break; Fracture

  AS REPORTED, "NAIL AND SCREW BREAKAGE OF ALPHA GT FEMORAL NAIL. PATIENT WAS REFERRED FROM ER WITH BROKEN HARDWARE AROUND NONUNION SITE OF A FORMER PROXIMAL FEMORAL FRACTURE. SURGERY WAS PERFORMED TO REMOVE HARDWARE AND REPLACE IN ORDER TO ACHIEVE UNION."

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

  MAUDE report 16225506 ↗