AUTOBAHN 1257.8375Recalls & reported problems
Globus Medical, Inc. · AUTOBAHN EVO Locking Screw, 5x75mm, Ti · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00193982485993), received between Feb 19, 2025 and May 26, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Migration” (2 reports).
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Migration2
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Spinal Column Injury1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 26, 2026Migration
IT WAS REPORTED THAT THE PATIENT HAD ORIGINAL SURGERY FOR A LEFT DISTAL FEMUR FRACTURE (B)(6) 2026. THE PATIENT ORIGINALLY HAD A 14X380 RETROGRADE SFX NAIL INSERTED. AT PATIENT'S FOLLOW-UP IT WAS NOTICED WITHOUT IMAGING THAT ONE OF THE DISTAL SCREWS WAS BACKING OUT AND PUSHING AGAINST PATIENT'S SKIN; IT WAS CONFIRMED WITH IMAGING. DURING THE REVISION TODAY, THE BACKED-OUT SCREW WAS REMOVED, AND AN AUTOBAHN EVO HEADLESS SCREW WAS INSERTED. THE PATIENT REPORTED NO FALL OR ANY INCIDENT THAT MIGHT HAVE CAUSED ADDITIONAL TRAUMA POST INITIAL SURGERY.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 25284399 ↗MalfunctionFeb 19, 2025Migration; Migration
IT WAS REPORTED THAT A REVISION WAS NEEDED TO REPLACE AN AUTOBAHN EVO LOCKING SCREW THAT BACKED OUT POST OPERATIVELY.
Patient problems: Spinal Column Injury
MAUDE report 21413372 ↗
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- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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