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Brigade 7881001Recalls & reported problems

Nuvasive, Inc. · Brigade Plate Fix Pin, 12mm Threaded · Class 1

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 00887517162670), received between Dec 20, 2019 and Dec 20, 2019 — classified as 1 injury.

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Fracture1
  • Migration or Expulsion of Device1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryDec 20, 2019Fracture; Migration or Expulsion of Device; Fracture; Migration or Expulsion of Device

    ADDITIONAL INFORMATION RECEIVED FROM PATIENT STATING PATIENT WAS EXPERIENCING PAIN AND UNDERWENT A RECONSTRUCTIVE PROCEDURE AT L4 AND L5, S1 WHERE THE BONE GROWTH MATERIAL DID NOT TAKE. IT IS UNKNOWN WHEN THE REVISION PROCEDURE OCCURRED.

    Patient problems: Failure of Implant

    MAUDE report 9505453 ↗

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Sources and updates

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