Skip to content

NA 04.033.271SRecalls & reported problems

Synthes GmbH · 12MM / TI CANN FRN / GT 400MM / LEFT - STERILE · 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 10886982271914), received between Mar 2, 2023 and Mar 2, 2023 — classified as 1 injury.

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

  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryMar 2, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT ON (B)(6) 2023, DUE TO PATIENT INFECTION A REVISION SURGERY OF FEMORAL RECON NAIL(FRN) AND SCREWS TOOK PLACE. THIS REPORT IS FOR ONE (1) 12MM / TI CANN FRN / GT 400MM / LEFT - STERILE. THIS IS REPORT 1 OF 5 FOR COMPLAINT (B)(4).

    Patient problems: Unspecified Infection

    MAUDE report 16472728 ↗

Other ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices

All ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page