T2 1826-1340SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540379290), received between Feb 5, 2019 and Feb 5, 2019 — 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.

• InjuryFeb 5, 2019Fracture

  THIS PI IS FOR THE REVISION OF THE T2 NAIL. WHILE REPORTING A REVISION OF PATIENT'S LEFT KNEE, REP REPORTED THAT AFTER PATIENT HAD KNEE IMPLANTED, PATIENT FELL AND SUSTAINED A FEMORAL FRACTURE. A T2 NAIL WAS IMPLANTED TO ADDRESS THE FRACTURE AND WAS LATER REMOVED AT AN UNKNOWN DATE FOR AN UNKNOWN REASON.

  Patient problems: Fall

  MAUDE report 8304870 ↗