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STALIF C ABS1440Recalls & reported problems

Centinel Spine, LLC · Class 2

All models of STALIF C (3)

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

Adverse event reports
9
Deaths reported
0
Injuries reported
9
Recalls naming it
0

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00815101029016), received between May 24, 2021 and May 24, 2021 — classified as 9 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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem9

Patient problems

  • Bone Fracture(s)9

Recent adverse event reports

The 9 most recent of 9 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 11869832 ↗
  • 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 11869831 ↗
  • 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 11869830 ↗
  • 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 11869829 ↗
  • 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 11869828 ↗
  • 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 11869827 ↗
  • 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 11869826 ↗
  • 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 11869823 ↗
  • 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 11869821 ↗

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Sources and updates

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