RESONATE 1194.3048Recalls & reported problems
Globus Medical, Inc. · RESONATE Anterior Cervical Plate, 3-Level, 48mm · Class 2 · Implant
All models of RESONATE (24)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00193982155377), received between Nov 4, 2022 and Apr 24, 2026 — classified as 2 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Migration” (4 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
- Migration4
- Device Slipped1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Dysphasia1
- Implant Pain1
- No Clinical Signs, Symptoms or Conditions1
- Pain1
- Spinal Cord Injury1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryApr 24, 2026Migration
IT WAS REPORTED THAT THERE WAS A RESONATE REVISION. THE RESONATE SCREW BACKED OUT OF PLATE FROM A PREVIOUS SURGERY ON (B)(6) 2022. WE REPLACED THE PLATE AND SCREWS WITH XTEND.
Patient problems: Dysphasia; Pain
MAUDE report 24981159 ↗InjuryNov 11, 2025Migration; Migration
IT WAS REPORTED THAT A 3 LEVEL RESONATE PLATE HAD A SCREW BACK OUT TO THE POINT THE SCREW WAS SITTING 9.1MM PROUD. THE PT CAME INTO ER COMPLAINING OF SEVERE PAIN WHEN SWALLOWING AND DISCOMFORT. THE SCREW BLOCKING MECHANISM SEEMS TO BE BROKEN/DAMAGED IN 4 SCREW HOLES.
Patient problems: Implant Pain
MAUDE report 23526038 ↗MalfunctionJul 18, 2024Migration; Migration
IT WAS REPORTED THAT RESONATE SCREWS ARE BACKING OUT OF THE PLATE 6 WEEKS POST-OPERATIVELY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19776845 ↗MalfunctionMar 19, 2024Migration; Migration
IT WAS REPORTED THAT SCREWS ARE BACKING OUT OF A RESONATE PLATE POST OPERATIVELY.
Patient problems: Spinal Cord Injury
MAUDE report 18935123 ↗MalfunctionNov 4, 2022Device Slipped
IT WAS REPORTED THAT A REVISION SURGERY WAS DONE TO REMOVE AND REPLACE (8) SCREWS, DUE TO 2 SCREWS BACKING OUT OF A RESONATE PLATE 7 MONTHS POST-OPERATIVELY.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 15733986 ↗
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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