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MectaLIF Anterior 03.30.303Recalls & reported problems

Medacta International SA · MectaLIF Ant - Lag Plate Flush H16 mm · Class 2 · Implant

All models of MectaLIF Anterior (6)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

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.

Recalls naming this device

  1. Mar 8, 2023Class IICompleted

    There is a potential for breakage of the small screw used to affix the anti-backout plate.

    Z-1403-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

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Sources and updates

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