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STALIF C-Ti C145541-3TcRecalls & reported problems

Centinel Spine, LLC · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00815101028651), received between May 24, 2021 and May 24, 2021 — classified as 1 injury.

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 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 24, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    A PATIENT RECEIVED 3 LEVELS OF STALIF C-TI INTERBODY CAGES AND ABO SCREWS AT C3/4, C5/6, AND C6/7 ON (B)(6) 2021. ON AN UNKNOWN DATE, THE PATIENT PRESENTED WITH A COLLAPSED C6 VERTEBRAE IDENTIFIED VIA LATERAL X-RAY. ON (B)(6) 2021, THE PATIENT WAS REVISED TO A C6 CORPECTOMY BY REMOVAL OF 2 OF THE 3 STALIF C-TI CAGES.

    Patient problems: Bone Fracture(s)

    MAUDE report 11869824 ↗

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Sources and updates

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