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TRIGEN 71675266Recalls & reported problems

Smith & Nephew, Inc. · TRIGEN INTERTAN 10MM X 34CM 130DEGREE RIGHT · Class 2 · Implant

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03596010560896), received between Jul 31, 2018 and May 27, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Fracture” (1 report).

6 other recalls cover devices cleared under the same FDA submission (K040212); they may or may not involve this specific model.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Fracture1
  • Insufficient Device Problem Information1
  • Migration1

Patient problems

  • Injury1
  • Intraoperative Pain1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 27, 2019Fracture; Fracture

    IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED ON THE PATIENT DUE TO THE BREAKAGE OF THE INTERTAN NAIL.

    Patient problems: Injury

    MAUDE report 8643563 ↗
  • InjuryJul 31, 2018Insufficient Device Problem Information; Migration; Insufficient Device Problem Information; Migration

    IT WAS REPORTED A REVISION SURGERY IN WHICH THE COMPRESSION SCREW BACKED OFF THREE MONTHS POST-OP. THEY HAD TO REMOVE THE NAIL BECAUSE THE PROMINENT SCREW CAUSED PAIN. ALL PIECES WERE REMOVED.

    Patient problems: Intraoperative Pain

    MAUDE report 7737678 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K040212. One submission often covers many models, so check the product and lot details in each record.

  • Z-1133-2022 · Apr 22, 2022 · Open, Classified
    INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
  • Z-0772-2021 · Nov 2, 2020 · Terminated
    Bone fixation nail. TRIGEN INTERTAN - Product Usage: indicated for fractures of the femur including simple shaft fractures, comminuted shaft fractures, spiral shaft fractures, long
  • Z-0097-2018 · Oct 24, 2017 · Open, Classified
    smith&nephew TRIGEN INTERTAN 10S, REF 71675384, 10 MM X 18 CM NAIL, 130o (degrees), SET SCREW PREASSEMBLED IN NAIL
  • Z-2258-2014 · Jul 2, 2014 · Terminated
    TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL, 125o, REF 71675201, QTY (1), STERILE R, Smith & Nephew, Memphis, Inc., TN 38116 TRIGEN(R) INTERTAN(TM) 11.5MM X 18 CM NAIL, 125o, REF 71
  • Z-1637-2014 · Apr 4, 2014 · Terminated
    TRIGEN INTERTAN 1.5 NAIL: (1) REF 71676515, 10 MM X 10 CM, 125 degree, LEFT, (2) REF 71676556, 11.5 MM X 36 CM, 125 degree, RIGHT, (3) REF 71676558, 11.5 MM X 38 CM, 125 degree
  • Z-1636-2014 · Apr 4, 2014 · Terminated
    TRIGEN INTERTAN NAIL: (1) REF 71675201, 10 MM X 18 CM, 125 degree, (2) REF 71675202, 11.5 MM X 18 CM, 125 degree, (3) REF 71675203, 13 MM X 18 CM, 125 degree, (4) REF 71675204,

Other NAIL, FIXATION, BONE devices

All NAIL, FIXATION, BONE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.