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LCS COMPLETE 1294-12-030Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE RPS Flexion Femoral CEMENTED MED LEFT · Class 3 · Implant

All models of LCS COMPLETE (117)

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 10603295022916), received between Nov 2, 2018 and Nov 2, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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

  • Appropriate Device Problem Term/Code Not Available1
  • Loose or Intermittent Connection1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryNov 2, 2018Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available; Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available

    PATIENT WAS REVISED TO ADDRESS PAIN AND LOOSENING OF THE TIBIAL AND FEMORAL COMPONENTS AT BONE TO CEMENT AND CEMENT TO IMPLANT INTERFACE.

    Patient problems: Pain

    MAUDE report 8033610 ↗

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

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Sources and updates

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