T2 ALPHA 2333-1032SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327285970), received between May 14, 2021 and May 14, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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.

• InjuryMay 14, 2021Fracture; Fracture

  THE FOLLOWING WAS REPORTED: THE T2ALPHA GT NAIL WAS INSERTED ON (B)(6) 2020. THE PATIENT WAS COMPLAINING OF PAIN IN THE PROXIMAL FEMUR WHEN HE VISITED THE HOSPITAL IN MID-(B)(6), AND WHEN THE X-RAY WAS CHECKED, IT WAS CONFIRMED THAT THE NAIL WAS BROKEN. IT WAS NOT A FACTOR SUCH AS A FALL, BUT (B)(6) 2021 RE-OPERATION WAS PERFORMED, THE T2 ALPHA WAS PULLED OUT, A LONG GAMMA WAS INSERTED, AND ANOTHER COMPANY'S PLATE WAS INSERTED.

  Patient problems: Failure of Implant; Impaired Healing; Implant Pain

  MAUDE report 11825147 ↗