T2 2339-1240SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327293098), received between Dec 20, 2022 and Dec 20, 2022 — 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.

• InjuryDec 20, 2022Break; Fracture; Break; Fracture

  AS REPORTED: "PATIENT RETURNED TO CLINIC AFTER EXPERIENCING PAIN. X-RAYS WERE TAKEN AND SHOWED THE NAIL HAD BROKEN AND NONUNION. AN INITIAL EXPLANT REMOVAL SURGERY WITH I&D TOOK PLACE ON (B)(6) 2022. THEN A REVISION SURGERY FOLLOWED AND A STANDARD SCN NAIL WAS IMPLANTED ON (B)(6) 2022."

  Patient problems: Failure of Implant; Implant Pain; Nonunion/Delayed-union Bone Fracture

  MAUDE report 16012791 ↗