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XLIF 3230093Recalls & reported problems

Nuvasive, Inc. · XLIF Corpectomy Osteotome, 25mm · 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 00887517504180), received between Dec 16, 2020 and Dec 16, 2020 — 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

  • Paralysis1

Recent adverse event reports

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

  • InjuryDec 16, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    ON (B)(6) 2020, THE PATIENT UNDERWENT A SPINAL PROCEDURE TO REPLACE T12 TO L1. IMMEDIATELY POST-OP THE PATIENT REPORTEDLY DEVELOPED PARALYSIS. ON (B)(6) 2020, IT WAS REPORTED THAT THE PATIENT WAS STILL EXPERIENCING PARALYSIS. NO DURAL DAMAGE IDENTIFIED, SO PHYSICIAN COMMENTED CAUSE OF PARALYSIS MAY BE THE RESULT OF SPINAL CORD DAMAGED WHILE UTILIZING AN OSTEOTOME AT T12. ON (B)(6) 2020, IT WAS REPORTED THAT THE PATIENT¿S LEFT LIMB WAS RECOVERING BUT THE RIGHT LIMB WAS NOT.

    Patient problems: Paralysis

    MAUDE report 11019636 ↗

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Sources and updates

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