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LCS 1278-51-025Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS TIBIAL INSERT ROTATING PLATFORM BRIDGING BEARING STD+/LG 10mm · Class 3 · Implant

All models of LCS (45)

Data updated Oct 16, 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 10603295020639), received between Mar 11, 2019 and Mar 11, 2019 — 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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • No Code Available1
  • Pain1

Recent adverse event reports

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

  • InjuryMar 11, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    PATIENT WAS REVISED TO ADDRESS PAIN. RESURFACED PATELLA AND EXCHANGE OF POLY WAS DONE. DOI: (B)(6) 1998; DOR: (B)(6) 2019, LEFT KNEE.

    Patient problems: No Code Available; Pain

    MAUDE report 8408903 ↗

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

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Sources and updates

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