RESONATE 1194.2030Recalls & reported problems
Globus Medical, Inc. · RESONATE Anterior Cervical Plate, 2-Level, 30mm · Class 2 · Implant
All models of RESONATE (24)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00193982154813), received between Nov 22, 2021 and Jan 12, 2026 — classified as 1 injury, 3 malfunctions.
The most frequently reported specific device problem is “Human-Device Interface Problem” (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.
Reports received per month
Most reported problems
Device problems
- Human-Device Interface Problem2
- Break1
- Insufficient Device Problem Information1
- Migration1
Patient problems
- Failure of Implant1
- Insufficient Information1
- Spinal Column Injury1
- Unspecified Tissue Injury1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryJan 12, 2026Human-Device Interface Problem
IT WAS REPORTED THE BOTTOM RESONATE SCREW WAS BACKING OUT OF THE CONSTRUCT.
Patient problems: Failure of Implant
MAUDE report 24037745 ↗MalfunctionNov 5, 2024Break; Migration; Break; Migration
IT WAS REPORTED THAT A REVISION WAS NEEDED TO REPLACE RESONATE SCREWS BACKING OUT OF THE PLATE POST-OPERATIVELY.
Patient problems: Insufficient Information
MAUDE report 20610266 ↗MalfunctionMar 1, 2024Human-Device Interface Problem; Human-Device Interface Problem
IT WAS REPORTED THAT SCREWS ARE BACKING OUT OF A RESONATE PLATE POST OPERATIVELY.
Patient problems: Spinal Column Injury
MAUDE report 18821881 ↗MalfunctionNov 22, 2021Insufficient Device Problem Information
IT WAS REPORTED THAT A PATIENT IS EXPERIENCING ADVERSE AFFECTS AFTER A SURGERY INVOLVING RESONATE.
Patient problems: Unspecified Tissue Injury
MAUDE report 12855875 ↗
Other Appliance, fixation, spinal intervertebral body devices
- CD HORIZON® SOLERA® VOYAGER™ Spinal System 6550017Medtronic Sofamor Danek, Inc. · Appliance, fixation, spinal intervertebral body131 reports
- 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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