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Mecta-C Cervical Ti-Peek Cages 03.28.722Recalls & reported problems

Medacta International SA · Cervical Interbody Fusion Device Dome Shaped 14x16x7 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 07630030833045), received between Feb 18, 2022 and Feb 18, 2022 — 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

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Implant Pain1

Recent adverse event reports

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

  • InjuryFeb 18, 2022Appropriate Device Problem Term/Code Not Available

    HE CAGE WAS REVISED 1 WEEK AFTER THE PRIMARY FOLLOWING SUSPECTED CERVICALGIA AND PAINFUL-SENSORY C6 RADICULOPATHY LEFT.

    Patient problems: Implant Pain

    MAUDE report 13558599 ↗

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Sources and updates

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