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XLIF 6910222Recalls & reported problems

Nuvasive, Inc. · XLIF Cobb, Straight Small · Class 1

All models of XLIF (9)

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 00887517390509), received between Jun 7, 2018 and Jun 7, 2018 — 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

  • Damage to Ligament(s)1

Recent adverse event reports

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

  • InjuryJun 7, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    ON (B)(6) 2018, A PATIENT UNDERWENT AN EXTREME LATERAL INTERBODY FUSION PROCEDURE AT L2-L5 LEVELS. DURING THE PROCEDURE THE ANTERIOR LONGITUDINAL LIGAMENT WAS DAMAGED AT L4/L5 LEVEL. AS PER REPORTER CAGES WERE IMPLANTED WITH NO ISSUED IN LEVELS L2-L4, BUT AFFECTED LEVEL WAS PACKED WITH BONE PROSTHESIS ANTERIORLY AUTOGENOUS BONE POSTERIORLY.

    Patient problems: Damage to Ligament(s)

    MAUDE report 7578696 ↗

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Sources and updates

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