T2 ALPHA 2331-0938SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327284713), received between Feb 17, 2022 and Feb 17, 2022 — 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 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.

• InjuryFeb 17, 2022Break; Fracture; Break; Fracture

  "PATIENT REPORTED SHE WAS WALKING WHEN SHE FELT A SNAP IN HER LEG. SHE REPORTED SHE FELT PAIN IN HER LEG FOR A WEEK BEFORE THE EVENT. AFTER FURTHER FOLLOW EVALUATION, RESULTS SHOWED THE PROXIMAL END OF THE ANTEGRADE FEMORAL NAIL HAD BROKEN NEAR THE LEVEL OF THE LAG SCREWS. REVISION SURGERY PERFORMED. REPLACEMENT DEVICE USED: GAMMA LONG NAIL WITH RC LAG SCREW."

  Patient problems: Failure of Implant; Implant Pain

  MAUDE report 13552894 ↗