AUTOBAHN 1257.8370Recalls & reported problems
Globus Medical, Inc. · AUTOBAHN EVO Locking Screw, 5x70mm, Ti · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00193982485979), received between Mar 5, 2024 and Apr 8, 2026 — classified as 3 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
- Product Quality Problem1
Patient problems
- Insufficient Information2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 8, 2026Migration
IT WAS REPORTED THAT THE PATIENT'S ORIGINAL SURGERY DATE WAS (B)(6) 2025. THE PATIENT HAD A 10X240 SFX RETROGRADE NAIL INSERTED AS WELL AS A SMITH & NEPHEW DISTAL FEMUR PLATE. WHEN PATIENT FOLLOWED UP IN CLINIC ON (B)(6) 2026, IMAGINE SHOWED THAT THE 80MM SCREW IN THE MOST DISTAL MEDIAL TO LATERAL HOLE WAS BACKED OUT. THE FRACTURE IS HEALED BUT SURGEON REMOVED THE SCREW TODAY ON (B)(6) 2026. DURING THE REVISION, IT WAS ALSO NOTICED THAT THE 70MM SCREW IN THE 2ND MOST PROXIMAL DISTAL SCREW WAS ALSO BACKED OUT SO HE REMOVED THAT AS WELL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24817406 ↗MalfunctionAug 8, 2024Migration; Migration
IT WAS REPORTED THAT A REVISION WAS NEEDED TO REPLACE AN AUTOBAHN SCREW THAT BACKED OUT OF THE NAIL 60+ DAYS POST-OPERATIVELY.
Patient problems: Insufficient Information
MAUDE report 19940955 ↗MalfunctionMar 5, 2024Product Quality Problem; Product Quality Problem
IT WAS REPORTED THAT A REVISION SURGERY WAS NEEDED DUE TO AN AUTOBAHN EVO LOCKING SCREW THAT WAS FOUND LOOSE POST OPERATIVELY.
Patient problems: Insufficient Information
MAUDE report 18837381 ↗
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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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