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LCS 1178-28-025Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS TIBIAL INSERT MENISCAL BEARING LG 10mm · 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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295007845), received between Feb 28, 2018 and Feb 28, 2018 — 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

  • Adverse Event Without Identified Device or Use Problem1

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.

  • InjuryFeb 28, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    REVISION PINNACLE, (B)(6) HOSPITAL (B)(6) 2018 UNKNOWN PRIMARY DATE, UNKNOWN 1ST REVISION DATE. REVISION (B)(6) 2018 LINER EXCHANGE OF LCS MENISCAL BEARING DUE TO INFECTION. SURGICAL TEAM REPORT SYSTEMIC INFECTION. INSERTS APPEAR UNDAMAGED ON REMOVAL. REPLACEMENT BEARING INSERTED. (B)(6) REP PRESENT FOR CASE, NO SUPPORTING DATA AVAILABLE. MALE PATIENT AGED (B)(6) YEARS. DOI: UNKNOWN: DOR: (B)(6) 2018; UNK HIP.

    Patient problems: Unspecified Infection

    MAUDE report 7302679 ↗

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Sources and updates

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