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LCS 1278-25-025Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS TIBIAL INSERT MENISCAL BEARING BRIDGING BEARING STD+/LG 12.5mm · Class 3 · Implant

All models of LCS (45)

Data updated Oct 18, 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 10603295020424), received between Mar 16, 2020 and Mar 16, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Naturally Worn” (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

  • Naturally Worn1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionMar 16, 2020Naturally Worn; Naturally Worn

    PATIENT HAS THIS IN-SITU. THERE IS NO COMPLAINT ISSUES, BUT NORMAL POLY WEAR AFTER 20YRS.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9835620 ↗

Other Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing devices

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Sources and updates

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