T2 ALPHA 2331-1136SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327284218), received between Sep 7, 2022 and Mar 24, 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.

• InjuryMar 24, 2023Break; Fracture; Break; Fracture

  AS REPORTED: "THE NAIL WAS IMPLANTED INTO THE PATIENT IN DECEMBER, 2022. BECAUSE THE PATIENT FELL DOWN AT THE END OF FEBRUARY AND IT WAS FOUND THAT THE NAIL WAS BROKEN, REOPERATION WAS PERFORMED ON (B)(6) 2023."

  Patient problems: Failure of Implant; Fall

  MAUDE report 16611181 ↗
• InjurySep 7, 2022Break; Fracture; Device Dislodged or Dislocated; Break; Fracture; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT WAS 3-MONTH'S STATUS POST ANTEGRADE NAILING OF A LEFT PROXIMAL FEMORAL SUBTROCHANTERIC FRACTURE. THE PATIENT HAD A SCREW DISENGAGEMENT OF BOTH OF THE DISTAL INTERLOCKS WITH PAINFUL HARDWARE. THIS RESULTED IN THE DEVICE BEING REMOVED.

  Patient problems: Failure of Implant; Implant Pain

  MAUDE report 15369536 ↗