Brigade 7806535Recalls & reported problems
Nuvasive, Inc. · Brigade® Plate Screw 6.5x35.0mm · Class 2 · Implant
All models of Brigade (17)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887517141804), received between Nov 5, 2018 and Nov 5, 2018 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (2 reports).
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
- Fracture2
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 5, 2018Fracture; Fracture
ON AN UNKNOWN DATE A PATIENT UNDERWENT AN ANTERIOR LUMBAR INTERBODY FUSION PROCEDURE AT L5-S1 LEVELS. POST-OPERATIVE RADIOGRAPHS SHOWED A SCREW FRACTURE AT S1 LEVEL. THE PATIENT WAS FUSED AND HAS IS ASYMPTOMATIC. NO REVISION PROCEDURE IS PLANNED AT THIS TIME.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8040373 ↗MalfunctionNov 5, 2018Fracture; Fracture
ON AN UNKNOWN DATE A PATIENT UNDERWENT AN ANTERIOR LUMBAR INTERBODY FUSION PROCEDURE AT L5-S1 LEVELS. POST-OPERATIVE RADIOGRAPHS SHOWED A SCREW FRACTURE AT S1 LEVEL. THE PATIENT WAS FUSED AND HAS IS ASYMPTOMATIC. NO REVISION PROCEDURE IS PLANNED AT THIS TIME.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8040342 ↗
Other APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY devices
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- EVEREST® Spinal System 2901-10001VB Spine LLC · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY119 reports
- ZEVO™ Anterior Cervical Plate System 7710015Medtronic Sofamor Danek, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall1 report
- Mariner RDX MX1-000040Seaspine Orthopedics Corporation · Appliance, fixation, spinal intervertebral body1 recall0 reports
- Mariner RDX MX1-000030Seaspine Orthopedics Corporation · Appliance, fixation, spinal intervertebral body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430112Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430224Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- XLP 7565050Nuvasive, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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