RESONATERecalls & reported problems across all models
Globus Medical, Inc. · 24 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 52
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls
- 0
We found 24 models of RESONATE by Globus Medical, Inc. in the FDA's device registry (GUDID). Together they are named in 52 adverse event reports in the FDA's MAUDE database, received between Sep 23, 2020 and Apr 24, 2026 — classified as 3 injuries, 49 malfunctions.
The most frequently reported specific device problem is “Migration” (17 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported RESONATE problems
Device problems
- Migration17
- Device Slipped10
- Break6
- Device Dislodged or Dislocated6
- Human-Device Interface Problem3
- Loose or Intermittent Connection3
- Improper or Incorrect Procedure or Method2
- Connection Problem1
Patient problems
- Insufficient Information22
- No Clinical Signs, Symptoms or Conditions12
- Failure of Implant8
- Spinal Column Injury4
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
- Dysphasia1
- Implant Pain1
- Pain1
RESONATE models
24 models, most reported first. Each model has its own page with its reports, recalls and device details.
- RESONATE 1194.3048Appliance, fixation, spinal intervertebral body5 reports
- RESONATE 1194.3051Appliance, fixation, spinal intervertebral body5 reports
- RESONATE 1194.2028Appliance, fixation, spinal intervertebral body4 reports
- RESONATE 1194.2030Appliance, fixation, spinal intervertebral body4 reports
- RESONATE 1194.3045Appliance, fixation, spinal intervertebral body4 reports
- RESONATE 1194.2032Appliance, fixation, spinal intervertebral body3 reports
- RESONATE 1194.2034Appliance, fixation, spinal intervertebral body3 reports
- RESONATE 1194.3042Appliance, fixation, spinal intervertebral body3 reports
- RESONATE 1194.7216Appliance, fixation, spinal intervertebral body2 reports
- RESONATE 1194.2036Appliance, fixation, spinal intervertebral body2 reports
- RESONATE 1194.3054Appliance, fixation, spinal intervertebral body2 reports
- RESONATE 1194.3148Appliance, fixation, spinal intervertebral body2 reports
- RESONATE 1194.3154Appliance, fixation, spinal intervertebral body2 reports
- RESONATE 1194.7214Appliance, fixation, spinal intervertebral body1 report
- RESONATE 1194.1010Appliance, fixation, spinal intervertebral body1 report
- RESONATE 1194.1014Appliance, fixation, spinal intervertebral body1 report
- RESONATE 1194.2020Appliance, fixation, spinal intervertebral body1 report
- RESONATE 1194.2130Appliance, fixation, spinal intervertebral body1 report
- RESONATE 1194.2136Appliance, fixation, spinal intervertebral body1 report
- RESONATE 1194.3039Appliance, fixation, spinal intervertebral body1 report
- RESONATE 1194.3145Appliance, fixation, spinal intervertebral body1 report
- RESONATE 1194.4057Appliance, fixation, spinal intervertebral body1 report
- RESONATE 1194.4060Appliance, fixation, spinal intervertebral body1 report
- RESONATE 1194.4069Appliance, fixation, spinal intervertebral body1 report
Recent RESONATE adverse event reports
The 15 most recent reports across all models, 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 ↗MalfunctionMar 30, 2026Migration
IT WAS REPORTED THAT THE SCREW BACKED OUT OF RESONATE PLATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24735047 ↗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 ↗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 ↗MalfunctionMay 2, 2025Migration; Migration
IT WAS REPORTED THAT DURING A REVISION, RESONATE SCREWS WERE BACKING OUT OF THE PLATE POST-OPERATIVELY.
Patient problems: Spinal Column Injury
MAUDE report 21951300 ↗MalfunctionNov 13, 2024Migration; Migration
IT WAS REPORTED THAT A REVISION WAS NEEDED TO REPLACE RESONATE SCREWS BACKING OUT OF THE PLATE POST-OPERATIVELY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20677696 ↗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 ↗MalfunctionNov 5, 2024Migration; Migration
IT WAS REPORTED THAT RESONATE SCREWS ARE BACKING OUT OF THE PLATE POST-OPERATIVELY.
Patient problems: Insufficient Information
MAUDE report 20610227 ↗MalfunctionOct 25, 2024Migration; 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 20538314 ↗MalfunctionSep 27, 2024Migration; Migration
IT WAS REPORTED THAT A REVISION SURGERY WAS NEEDED TO REPLACE SCREWS THAT BACKED OUT OF A RESONATE PLATE POST-OPERATIVELY.
Patient problems: Insufficient Information
MAUDE report 20320415 ↗MalfunctionSep 11, 2024Migration; Migration
IT WAS REPORTED THAT RESONATE SCREWS ARE BACKING OUT OF THE PLATE POST-OPERATIVELY.
Patient problems: Insufficient Information
MAUDE report 20192630 ↗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 ↗MalfunctionJul 18, 2024Migration; Migration
IT WAS REPORTED THAT RESONATE SCREWS ARE BACKING OUT OF THE PLATE POST-OPERATIVELY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19776742 ↗MalfunctionJul 12, 2024Migration; Migration
IT WAS REPORTED THAT A REVISION SURGERY WAS NEEDED TO REPLACE SCREWS THAT BACKED OUT OF A RESONATE PLATE POST-OPERATIVELY.
Patient problems: Spinal Column Injury
MAUDE report 19734542 ↗MalfunctionJul 12, 2024Migration; Migration
IT WAS REPORTED THAT A REVISION SURGERY WAS NEEDED TO REPLACE SCREWS THAT BACKED OUT OF A RESONATE PLATE POST-OPERATIVELY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19734433 ↗
Other Globus Medical, Inc. products
All Globus Medical, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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