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MectaLIF Anterior System 03.31.002Recalls & reported problems

Medacta International SA · Anterior Interbody Fusion Device 24x31x12 L5° · Class 2 · Implant

All models of MectaLIF Anterior System (12)

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630030833755), received between Jun 7, 2018 and Jun 7, 2018 — classified as 1 malfunction.

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 Problem1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionJun 7, 2018Adverse Event Without Identified Device or Use Problem

    DURING AN L4-S1 ALIF CASE, WHEN THE SURGEON WAS TRIALING THE CAGE HE INFORMED THE SALES AGENT THAT HE DOES NOT LIKE THE SHAPE OF THE TRIALS/IMPLANT. THE SURGEON DOWNSIZED THE CAGE AND IMPLANTED A 24X31X12 BECAUSE THE CAGES ARE TOO SQUARE. THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7578042 ↗

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Sources and updates

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