Traverse 7820050Recalls & reported problems
Nuvasive, Inc. · Traverse Plate, Size 50 Fixed · Class 2 · Implant
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 00887517152954), received between Jun 12, 2023 and Jun 12, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (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
- Migration1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 12, 2023Migration; Migration
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL CORPECTOMY PROCEDURE WITH PLATE FIXATION AT L2. SUBSEQUENTLY, IT WAS REPORTED THAT THE PATIENT SUFFERED A FALL RESULTING IN MIGRATION OF THE PLATE COMPONENT. THE PATIENT UNDERWENT A REVISION PROCEDURE APPROXIMATELY FOUR (4) WEEKS LATER TO REMOVE THE PLATE CONSTRUCT. THE PROCEDURE WAS COMPLETED WITHOUT REPLACEMENT OF THE PLATE FIXATION COMPONENTS, ONLY THE CORPECTOMY CAGE WAS LEFT IN PLACE. IT WAS NOTED THAT THE PATIENT EXPERIENCED A CAR ACCIDENT APPROXIMATELY 30 YEARS PRIOR, RESULTING IN SEVERAL PROBLEMS INCLUDING UNILATERAL WEAKNESS. NO FURTHER PATIENT IMPACT WAS REPORTED. NO ADDITIONAL INFORMATION WAS AVAILABLE.
Patient problems: Fall
MAUDE report 17111424 ↗
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- 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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