Skip to content

SECURE-C 714.266SRecalls & reported problems

Globus Medical, Inc. · SECURE-C Endplate & Core Assembly, 13x14, 6&deg, 6mm · Class 3 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889095179118), received between Jan 19, 2021 and Oct 24, 2022 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Output Problem” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Output Problem1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
  • Pain1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 24, 2022Output Problem

    IT WAS REPORTED THAT A REVISION SURGERY WAS COMPLETED TO REMOVE A SECURE C IMPLANT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 15657273 ↗
  • InjuryJan 19, 2021Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A REVISION SURGERY WAS DONE TO REMOVE A SECURE C DEVICE DUE TO PATIENT PAIN AND THE DEVICE BEING PLACED OFF MIDLINE.

    Patient problems: Pain

    MAUDE report 11195707 ↗

Other PROSTHESIS, INTERVERTEBRAL DISC devices

All PROSTHESIS, INTERVERTEBRAL DISC devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page