T2 1825-0936SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540199386), received between Dec 9, 2025 and Dec 9, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Use of Device Problem” (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 9, 2025Use of Device Problem; Use of Device Problem

  AS REPORTED: "A TRAUMA PATIENT WAS TREATED FOR A MID-SHAFT FEMUR FRACTURE WITH THE T2 FEMORAL AR NAIL IMPLANT. THE FRACTURE WAS REDUCED, AND THE FEMUR WAS DISTALLY REAMED TO 10.5MM TO ACCOMMODATE A 9 × 360 MM NAIL, WHICH WAS THE SMALLEST AVAILABLE SIZE. HOWEVER, THE IMPLANT FROM THE HOSPITAL¿S CONSIGNMENT INVENTORY HAD EXPIRED ON SEPTEMBER 30, 2025, AND A REPLACEMENT HAD NOT YET BEEN RECEIVED, MAKING IT UNAVAILABLE FOR USE. THE SURGERY TIME WAS EXTENDED BY MORE THAT 30 MINUTES AS THE TEAM REVIEWED SURGICAL OPTIONS AND PREPARED THE FEMUR TO IMPLANT A LARGER NAIL. ADDITIONAL REAMING WAS PERFORMED TO ACCOMMODATE A 10 × 360 MM T2 FEMORAL AR NAIL."

  Patient problems: Insufficient Information

  MAUDE report 23759581 ↗