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TRIGEN 71678080Recalls & reported problems

Smith & Nephew, Inc. · TRIGEN INTERTAN SUBTROCHANTERIC LAG SCREW 11MM X 80MM · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010565273), received between Aug 15, 2020 and Aug 15, 2020 — classified as 1 injury.

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

10 other recalls cover devices cleared under the same FDA submission (K040212, K210980); 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

  • Break1

Patient problems

  • Injury1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 15, 2020Break; Break

    IT WAS REPORTED THAT PATIENT WAS SCHEDULED TO HAVE THE SUBTROCH LAG SCREW EXPLANTED FROM AN INTERTAN ORIGINALLY DONE (B)(6) 2015. THE FRACTURE WAS HEALED AT THIS TIME. THE SURGEON HAD DIFFICULTY REMOVING THE SCREW AND THE SUBTROCHANTERIC DRIVER SHAFT ITEM 71674068 THREADED TIP BROKE OFF INSIDE OF THE SCREW THAT WAS REMOVED. NO FRAGMENTS WERE LEFT IN THE PATIENT. THE SURGEON WAS ALSO ATTEMPTING TO REMOVE THE INTERTAN NAIL, BUT WAS NOT ABLE TO REMOVE THE NAIL. THE SURGEON USED A POWERED CUTTING WHEEL TO REMOVE SOME OF THE PROXIMAL INTERTAN NAIL THAT WAS ABOUT 15MM PROUD, PRODRUDING FROM THE PATIENT¿S GREATER TROCHANTER.

    Patient problems: Injury

    MAUDE report 10411821 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K040212, K210980. One submission often covers many models, so check the product and lot details in each record.

  • Z-2456-2026 · Mar 16, 2026 · Open, Classified
    TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16, REF: 71760816
  • Z-1806-2025 · Mar 18, 2025 · Open, Classified
    META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
  • Z-2443-2023 · Jul 24, 2023 · Open, Classified
    TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT, REF 71647336, Femur nail
  • Z-2444-2023 · Jul 24, 2023 · Open, Classified
    TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT, REF 71647340, Femur nail
  • 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-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,
  • 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

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.