T2 2339-0930SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327292374), received between Oct 10, 2022 and Oct 10, 2022 — classified as 1 injury.

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.

• InjuryOct 10, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A DISTAL FEMUR FRACTURE TREATED WITH A SYNTHES PLATE BECAME INFECTED. THE PLATE WAS REMOVED AND THE DOCTOR WAITED FOR THE INFECTION TO CLEAR. ONCE IT WAS CLEAR, A 9MM T2 ALPHA RETROGRADE NAIL WAS INSERTED. THE NAIL FAILED AND ANOTHER DOCTOR REMOVED THE 9MM NAIL AND REPLACED IT WITH A LARGER DIAMETER T2 ALPHA RETROGRADE NAIL AND A DISTAL FEMUR PLATE. NO ISSUES HAVE BEEN REPORTED SINCE.

  Patient problems: Insufficient Information

  MAUDE report 15571758 ↗