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AUTOBAHN 1190.3036SRecalls & reported problems

Globus Medical, Inc. · AUTOBAHN Ti Antegrade/Retrograde Femoral Nail, 10x360mm, PF · 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 00889095951493), received between Apr 26, 2022 and Apr 26, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

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

  • Break1

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.

  • MalfunctionApr 26, 2022Break

    IT WAS REPORTED THERE WAS A REVISION SURGERY TO REPLACE AN AUTOBAHN RETRO FEMORAL NAIL THAT HAD BROKEN POST OPERATIVELY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14212929 ↗

Other NAIL, FIXATION, BONE devices

All NAIL, FIXATION, BONE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.