Skip to content

Brigade 6941438Recalls & reported problems

Nuvasive, Inc. · Brigade Implant, 14x38x28mm 8° · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517398741), received between Jun 21, 2023 and Jun 21, 2023 — classified as 1 malfunction.

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

Device problems

  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJun 21, 2023Fracture; Fracture

    IT WAS REPORTED THAT WHILE IMPACTING THE IMPLANT WITHIN THE DISC SPACE VIA INSERTER AND MALLET, THE IMPLANT FRACTURED. IT WAS REPORTED THAT PROPER SURGICAL TECHNIQUE WAS FOLLOWED. A NEW IMPLANT WAS USED TO SUCCESSFULLY COMPLETE THE PROCEDURE AND THERE WAS NO ADVERSE IMPACT TO THE PATIENT, USER, OR PROCEDURE. NO ADDITIONAL INFORMATION IS AVAILABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17176710 ↗

Other SPINAL VERTEBRAL BODY REPLACEMENT DEVICE devices

All SPINAL VERTEBRAL BODY REPLACEMENT DEVICE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.