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Mecta-C Cervical Ti-Peek Cages 03.28.719Recalls & reported problems

Medacta International SA · Cervical Interbody Fusion Device Dome Shaped 14x16x4 L5° · Class 2 · Implant

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 07630030833014), received between Jul 25, 2023 and Jul 25, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Device Appears to Trigger Rejection” (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 18, 2026.

Most reported problems

Device problems

  • Device Appears to Trigger Rejection1

Patient problems

  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryJul 25, 2023Device Appears to Trigger Rejection; Device Appears to Trigger Rejection

    REVISION SURGERY PERFORMED DUE TO INFECTION THAT CAUSED CAUDAL AND CRANIAL VERTEBRAL FRACTURE ABOUT 2 MONTHS AFTER THE PRIMARY SURGERY. THE CAGE WAS REPLACED.

    Patient problems: Unspecified Infection

    MAUDE report 17387948 ↗

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Sources and updates

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