NA 456.360SRecalls & reported problems
Synthes GmbH · 10MM/130 DEG TI CANN TROCH FIXATION NAIL 400MM/RIGHT-STER · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 10886982227324), received between Jun 22, 2021 and Jun 22, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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
- Break1
- Device-Device Incompatibility1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 22, 2021Break; Device-Device Incompatibility; Break; Device-Device Incompatibility
THE SURGEON HAD DIFFICULTY WITH THE SET SCREW LOCKING INTO THE LAG SCREW. AFTER MULTIPLE TRIES OF ATTEMPTING TO GET THE SET SCREW TO LOCK INTO THE LAG SCREW, THE SET SCREW WOULD NOT PERFORM THIS ACTION. WE THEN SET THE NAIL ONTO THE BACK TABLE AND TRIED TO DIAGNOSE THE ISSUE WITH THE SET SCREW. AFTER ANALYZING THE NAIL, IT WAS NOTED THERE WAS A BROKEN PIECE ON THE SET SCREW. THE PROCEDURE WAS COMPLETED WITH ANOTHER NAIL WITH A TEN (10) MINUTE SURGICAL DELAY. THE PATIENT IS REPORTEDLY DOING WELL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12044437 ↗
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 · Terminated11MM/130 Degree Titanium Trochanteric Fixation Nail 380MM/Right, Sterile
- Z-0375-2016 · Nov 2, 2015 · TerminatedTrochanteric 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 · Terminated10 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 · TerminatedLarge 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 · TerminatedTitanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and unstable fractures of the proximal femur.
- Z-0474-2014 · Jul 30, 2013 · TerminatedSynthes 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 · TerminatedSynthes Trauma Nail System. The devices are indication for bone fixation.
Other ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices
- NA 03.033.001Synthes GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES265 reports
- GAMMA 3125-1180SStryker GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES249 reports
- NA 03.037.026Synthes GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES225 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-075Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls2 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-045Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- TRIGEN 71674067Smith & Nephew, Inc. · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES201 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-050Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- PRECICE Intramedullary Limb Lengthening System LSB5-075Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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