TRIGEN 71675040Recalls & reported problems
Smith & Nephew, Inc. · INTERTAN NAIL CAP 0.0MM · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010524720), received between Dec 29, 2019 and Dec 29, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Incomplete or Inadequate Connection” (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
- Incomplete or Inadequate Connection1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 29, 2019Incomplete or Inadequate Connection; Incomplete or Inadequate Connection
IT WAS REPORTED THAT DURING SURGERY, THE COMPRESSION SCREW DID NOT ENTER THE BROCADE GUIDE AND SHOWED REBOUND TO ENTER THE SLIDING SCREW. AT THE END, NO COMPRESSION SCREW IS PLACED, DISTAL LOCKING WAS NOT PERFORMED, NAIL INSERTION ARCH WAS REMOVED, THE SLIDING SCREW BLOCKED AND 0 MM PLUG PLACEMENT WAS PERFORMED, WHICH ALSO DOES NOT FIT PROPERLY INTO THE INTERTAN INTRAMEDULLARY NAIL. NO INJURY REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9528703 ↗
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, ClassifiedTRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16, REF: 71760816
- Z-1806-2025 · Mar 18, 2025 · Open, ClassifiedMETA-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
- Z-2444-2023 · Jul 24, 2023 · Open, ClassifiedTRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT, REF 71647340, Femur nail
- Z-2443-2023 · Jul 24, 2023 · Open, ClassifiedTRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT, REF 71647336, Femur nail
- 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.