STALIF C-Ti C166549-3TcRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00815101028736), received between May 24, 2021 and May 24, 2021 — classified as 2 injuries.

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

Recent adverse event reports

The 2 most recent of 2 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 11869825 ↗
• 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 11869822 ↗