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LCS COMPLETE 1294-16-510Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE TIBIAL INSERT ROTATING PLATFORM LCS RPS 10mm STD+ · Class 3 · Implant

All models of LCS COMPLETE (117)

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 10603295023241), received between Nov 26, 2019 and Nov 26, 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.

  • InjuryNov 26, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT HAD PATELLA COMPONENT REVISED DUE TO PAINFUL KNEE AND POLY INSERT REPLACED DURING PARTIAL REVISION KNEE TODAY. DOI: (B)(6) 2009; DOR: (B)(6) 2019; RIGHT KNEE.

    Patient problems: No Code Available; Pain

    MAUDE report 9378738 ↗

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

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Sources and updates

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