TRIGEN 71675201Recalls & reported problems
Smith & Nephew, Inc. · TRIGEN INTERTAN 10MM X 18CM 125DEGREE · 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 03596010561046), received between Mar 28, 2017 and Dec 30, 2019 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Device Dislodged or Dislocated1
- Fracture1
- Malposition of Device1
- Migration or Expulsion of Device1
Patient problems
- Failure of Implant1
- Fall1
- Injury1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 30, 2019Fracture; Fracture
IT WAS REPORTED THAT REVISION SURGERY WAS PERFORMED DUE TO NAIL FRACTURE.
Patient problems: Injury
MAUDE report 9531717 ↗InjuryMar 28, 2017Migration or Expulsion of Device; Malposition of Device; Device Dislodged or Dislocated; Migration or Expulsion of Device; Device Dislodged or Dislocated
IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED ON PATIENT WITH A COGNITIVE IMPAIRMENT. AN ALLEGED FALL OCCURED ON (B)(6) 2017, HOWEVER THIS IS UNCERTAIN IN TERMS OF PATIENT'S DEMENTIA. IT WAS REPORTED THAT X-RAY SHOWED THAT THE LAG SCREW HAS TURNED ITSELF UP IN ACETABULUM.
Patient problems: Failure of Implant; Fall
MAUDE report 6438399 ↗
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, ClassifiedINTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
- Z-0772-2021 · Nov 2, 2020 · TerminatedBone 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, Classifiedsmith&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 · TerminatedTRIGEN(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 · TerminatedTRIGEN 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 · TerminatedTRIGEN 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
- NA 03.043.024Synthes GmbH · NAIL, FIXATION, BONE234 reports
- NA 03.010.440Synthes GmbH · NAIL, FIXATION, BONE70 reports
- TRIGEN 71676627Smith & Nephew, Inc. · NAIL, FIXATION, BONE1 recall2 reports
- TRIGEN 71676628Smith & Nephew, Inc. · NAIL, FIXATION, BONE1 recall0 reports
- NA 03.043.018Synthes GmbH · NAIL, FIXATION, BONE33 reports
- TRIGEN 71675383Smith & Nephew, Inc. · NAIL, FIXATION, BONE29 reports
- NA 03.010.441Synthes GmbH · NAIL, FIXATION, BONE27 reports
- NA 03.010.435Synthes GmbH · NAIL, FIXATION, BONE24 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.