T2 1845-1230SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540412775), received between May 22, 2018 and May 22, 2018 — 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.

• InjuryMay 22, 2018Fracture

  IT WAS REPORTED THAT ON (B)(6) 2017: THE T2RECON NAIL WAS IMPLANTED FOR FEMORAL TROCHANTERIC FRACTURE. IN (B)(6) 2018: THE PATIENT HAD PAIN (THE PATIENT DID NOT FALL DOWN) AND THE NAIL FRACTURE WAS OBSERVED IN HOSPITAL. ON (B)(6) 2018: FRACTURED T2 NAIL WAS REMOVED AND THE REVISION SURGERY WAS DONE WITH NON STRYKER NAIL.

  Patient problems: Pain

  MAUDE report 7531485 ↗