T2 2339-1236SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327292923), received between Feb 10, 2022 and Jan 7, 2025 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJan 7, 2025Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

  AS REPORTED: PRIMARY SURGERY WAS PERFORMED ON (B)(6) 2023. REVISION SURGERY WAS PERFORMED DUE TO NON-UNION ON (B)(6) 2024. DUE TO A LACK OF CONFIRMATION BY SALES REP, THE SURGEON, AND THE DISTRIBUTOR, A DIFFERENT INSTRUMENT AND IMPLANT WERE ARRIVED THAN THE ONE ORDERED BY SURGEON. THE IMPLANT AND INSTRUMENTATION WERE RE-ARRANGED AND THE SURGERY WAS DELAYED 2 HOURS. THE PATIENT WAS POST INDUCTION OF ANESTHESIA. THIS PI IS FOR THE REVISION SURGERY.

  Patient problems: Nonunion/Delayed-union Bone Fracture

  MAUDE report 21098526 ↗
• MalfunctionFeb 10, 2022Positioning Failure; Positioning Failure

  IT WAS REPORTED; "THE DOCTOR USED A T2 ALPHA RETROGRADE NAIL ON A PERIPROSTHETIC FRACTURE. WHEN IMPLANTING THE NAIL, THE FRACTURE WAS WELL REDUCED. WHEN THE NAIL WAS FULLY INSERTED IT KICKED THE FRACTURE INTO EXTENSION. HE WAS FRUSTRATED THAT HE DIDN'T USE A COMPETITOR'S NAIL WITH THE 10 DEG BEND. THERE'S NO IMMEDIATE CONSEQUENCES. THE FRACTURE JUST HAS A SMALLER CHANCE OF HEALING APPROPRIATELY SINCE IT IS NOW IN ABOUT 8 DEG OF EXTENSION."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13509386 ↗