T2 1846-0934SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613153318712), received between Oct 18, 2021 and Oct 18, 2021 — 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.

• InjuryOct 18, 2021Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT FOLLOWING A FALL, A PATIENT HAD HER T2 RECONSTRUCTION NAIL (T2G NAIL, D9, L340, REF 1846-0934S, LOT K055B06RA) EXPLANTED, WHICH WAS BROKEN. THE NAIL WAS INSTALLED ON (B)(6) 2021. UPDATE - (B)(6) 2021: REMOVAL OF THE NAIL UNDER GA AND INSERTION OF A SPECIFIC PROSTHESIS FOR COMPLEX FRACTURE OF THE TROCHANTERIC MASS.

  Patient problems: Failure of Implant; Fall

  MAUDE report 12652219 ↗