SECURE-C 714.166SRecalls & reported problems
Globus Medical, Inc. · SECURE-C Endplate & Core Assembly, 11x12, 6°, 6mm · Class 3 · Implant
Data updated Oct 13, 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 00889095179071), received between Feb 9, 2021 and Mar 4, 2024 — classified as 1 injury, 3 malfunctions.
The most frequently reported specific device problem is “Expulsion” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Expulsion1
- Material Separation1
- Migration1
- Therapeutic or Diagnostic Output Failure1
Patient problems
- Insufficient Information2
- Failure of Implant1
- Scar Tissue1
- Spinal Column Injury1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 4, 2024Material Separation; Material Separation
IT WAS REPORTED THAT THE SECURE-C CORE HAD DISASSOCIATED FROM THE ENDPLATES APPROXIMATELY TWO MONTHS POST-OPERATIVELY REQUIRING REVISION SURGERY.
Patient problems: Failure of Implant
MAUDE report 18832642 ↗MalfunctionSep 22, 2021Expulsion; Therapeutic or Diagnostic Output Failure
IT WAS REPORTED THAT A REVISION WAS DONE TO REMOVE A SECURE-C IMPLANT THAT HAD BEEN CRUSHED AND EJECTED DORSALLY POST OPERATIVELY.
Patient problems: Scar Tissue; Spinal Column Injury
MAUDE report 12515546 ↗InjuryAug 31, 2021Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED THAT A REVISION SURGERY WAS COMPLETED TO REMOVE A SECURE C IMPLANT.
Patient problems: Insufficient Information
MAUDE report 12395318 ↗MalfunctionFeb 9, 2021Migration
IT WAS REPORTED THAT A REVISION WAS DONE TO REMOVE A SECURE-C DEVICE THAT HAD MIGRATED ANTERIORLY.
Patient problems: Insufficient Information
MAUDE report 11300323 ↗
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- Simplify® Cervical Artificial DiscNuvasive, Inc. · Prosthesis, Intervertebral Disc1 recall12 reports
- Prodisc C 09.820.055SCentinel Spine, LLC · Prosthesis, Intervertebral Disc1 recall9 reports
- Simplify® Cervical Artificial DiscNuvasive, Inc. · Prosthesis, Intervertebral Disc1 recall4 reports
- Prodisc C SK PDSXL5Centinel Spine, LLC · Prosthesis, Intervertebral Disc1 recall3 reports
- Simplify® Cervical Artificial DiscNuvasive, Inc. · Prosthesis, Intervertebral Disc1 recall3 reports
- Simplify® Cervical Artificial DiscNuvasive, Inc. · Prosthesis, Intervertebral Disc1 recall3 reports
- Simplify® Cervical Artificial DiscNuvasive, Inc. · Prosthesis, Intervertebral Disc1 recall3 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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