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Brigade 6941238Recalls & reported problems

Nuvasive, Inc. · Brigade Implant, 12x38x28mm 8° · Class 2 · Implant

All models of Brigade (17)

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 00887517398475), received between Nov 16, 2022 and Nov 16, 2022 — 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

  • Laceration(s)1

Recent adverse event reports

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

  • InjuryNov 16, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED ON A CLINICAL STUDY THAT ON (B)(6) 2022 A PATIENT UNDERWENT A TRANSFORAMINAL INTERBODY FUSION. THE SURGEON IDENTIFIED A SMALL INCIDENTAL DUROTOMY THAT TOOK PLACE DURING SURGERY WHERE THE LIGAMENTUM HAD ADHERED TO THE DURA. A DURAGEN PATCH WAS PLACED AND COVERED WITH ADHERUS. THERE WAS NO EXTRAVASATION AFTER THE REPAIR.

    Patient problems: Laceration(s)

    MAUDE report 15810321 ↗

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Sources and updates

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