EIT TLIF cage TUI81032Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04260557776582), received between Jun 25, 2026 and Jun 25, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Migration” (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

Recent adverse event reports

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

• MalfunctionJun 25, 2026Migration

  IT WAS REPORTED THAT THIS WAS AN UNKNOWN SURGERY PERFORMED ON AN UNKNOWN DATE. WHEN THE DEVICE IN QUESTION WAS INSERTED INTO THE INTERVERTEBRAL SPACE, AN ATTEMPT WAS MADE TO POSITION IT ANTERIOR TO THE VERTEBRAL BODY. HOWEVER, THE DEVICE ADVANCED BEYOND THE INTENDED POSITION AND PROTRUDED ANTERIORLY FROM THE VERTEBRAL BODY. THE POSITIONING WAS ATTEMPTED MULTIPLE TIMES, BUT THE DEVICE COULD NOT BE PLACED AT THE INTENDED LOCATION AND THE DEVICE WAS REMOVED. THE PROCEDURE WAS COMPLETED USING AN ALTERNATIVE DEVICE WITHOUT ISSUES. THE SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT ANY SURGICAL DELAY. NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25619265 ↗