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NA 456.359SRecalls & reported problems

Synthes GmbH · 10MM/130 DEG TI CANN TROCH FIXATION NAIL 380MM/LEFT-STER · Class 2 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 10886982227317), received between Jan 9, 2018 and Jan 9, 2018 — classified as 1 injury.

7 other recalls cover devices cleared under the same FDA submission (K011857); 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • No Code Available1

Recent adverse event reports

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

  • InjuryJan 9, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A HARDWARE REMOVAL AND REVISION WAS PERFORMED ON (B)(6) 2017. THE PATIENT WAS ORIGINALLY IMPLANTED WITH A TROCHANTERIC FIXATION NAIL, HELICAL BLADE, AND UNKNOWN SCREWS ON A UNKNOWN DATE. THE PATIENT SUBSEQUENTLY EXPERIENCED A NON-UNION AND THESE PARTS WERE REMOVED. THE REMOVED DEVICES WERE INTACT. THE PATIENT WAS REVISED TO A PLATE. THERE WAS NO SURGICAL DELAY. NO INFORMATION REGARDING THE PATIENT STATUS AS WELL THE PROCEDURE STATUS WAS PROVIDED. THIS COMPLAINT INVOLVES THREE (3) PARTS. THIS REPORT IS FOR A NAIL. (B)(4).

    Patient problems: No Code Available

    MAUDE report 7175069 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K011857. One submission often covers many models, so check the product and lot details in each record.

  • Z-0604-2018 · Jul 21, 2017 · Terminated
    11MM/130 Degree Titanium Trochanteric Fixation Nail 380MM/Right, Sterile
  • Z-0375-2016 · Nov 2, 2015 · Terminated
    Trochanteric Fixation Nail- Advanced System-11MM/130 DEG TI CANN TFNA 420MM/Right Sterile (The TFN-ADVANCED Proximal Femoral Nailing System) The TFN-ADVANCED Proximal Femoral Naili
  • Z-0219-2015 · Oct 29, 2014 · Terminated
    10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM - Sterile: intended to treat stable and unstable fractures of the proximal femur
  • Z-0387-2014 · Jul 31, 2013 · Terminated
    Large Buttress Compression Nut For Blade Guide Sleeve TFN The Synthes Large Buttress Compression Nut For Blade Guide Sleeve TFN is intended to treat stable and unstable pertrocha
  • Z-0452-2014 · Jul 30, 2013 · Terminated
    Titanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and unstable fractures of the proximal femur.
  • Z-0474-2014 · Jul 30, 2013 · Terminated
    Synthes Trochanteric Fixation Nail As part of the Synthes Trochanteric Fixation Nail (TFN) System, the TFN Nail is intended to treat stable and unstable fractures of the proximal
  • Z-2058-2013 · Nov 2, 2012 · Terminated
    Synthes Trauma Nail System. The devices are indication for bone fixation.

Other Screw, fixation, bone devices

All Screw, fixation, bone devices →

Sources and updates

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