T2 1825-1138SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540199652), received between Apr 11, 2023 and Apr 11, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Difficult to Remove” (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.

• InjuryApr 11, 2023Material Fragmentation; Difficult to Remove; Material Fragmentation; Difficult to Remove

  IT WAS REPORTED: "WHEN TRYING TO KNOCK OUT A T2 FEMUR NAIL, THE KNOCKOUT THREAD IN THE NAIL BROKE OFF. REMOVAL OF THE NAIL WAS NO LONGER POSSIBLE. THE CUSTOMER IS CURRENTLY LOOKING FOR ALTERNATIVE WAYS TO REMOVE THE NAIL IN A NEXT STEP."

  Patient problems: Foreign Body In Patient; Nonunion/Delayed-union Bone Fracture

  MAUDE report 16713976 ↗