T2 1828-1234SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540200679), received between Dec 10, 2021 and Dec 10, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

• InjuryDec 10, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED THE FOLLOWING ISSUE: "POSTOPERATIVE LOOSENING OF THE END CAP OCCURRED IN A CASE OF RETROGRADE INSERTION OF A T2 FEMORAL NAIL." ADDITIONAL INFORMATION RECEIVED: REVISION SURGERY WAS PERFORMED DUE TO THE NON-UNION ONE AND A HALF YEARS AFTER THE INITIAL SURGERY. THE LOOSENED END CAP WAS DISCOVERED DURING PATIENT FOLLOW-UP (X-RAYS) AND WAS ALSO REMOVED AT THE TIME OF REVISION ON A HALF YEARS AFTER THE INITIAL SURGERY.

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

  MAUDE report 12976309 ↗