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LCS COMPLETE 1294-09-340Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE CRUCIFORM M/B PAT REPLACEMENT STD · Class 3 · Implant

All models of LCS COMPLETE (117)

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

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295022435), received between Aug 9, 2017 and Oct 22, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Naturally Worn” (2 reports).

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 Worn2

Patient problems

  • No Code Available1
  • No Information1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 22, 2020Naturally Worn; Naturally Worn

    IT WAS REPORTED THAT THERE WAS POLY WEAR.

    Patient problems: No Code Available

    MAUDE report 10717816 ↗
  • InjuryAug 9, 2017Naturally Worn; Naturally Worn

    DER STATES THAT STD 10 MM MENISCAL BEARINGS AND ST PATELLA POLY EXCHANGED FOR WEAR.

    Patient problems: No Information

    MAUDE report 6778302 ↗

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

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Sources and updates

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