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LCS COMPLETE 1294-11-030Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE RPS Flexion Femoral CEMENTED MED RIGHT · 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 10603295022848), received between Feb 1, 2021 and Feb 1, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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

  • Loss of or Failure to Bond1

Patient problems

  • Muscular Rigidity1
  • Pain1

Recent adverse event reports

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

  • InjuryFeb 1, 2021Loss of or Failure to Bond; Loss of or Failure to Bond

    CLINICAL NOTIFICATION RECEIVED FOR REVISION OF RIGHT TOTAL KNEE ARTHROPLASTY, TO ADDRESS ASEPTIC LOOSENING OF THE TIBIAL TRAY AND FEMUR, PAIN, AND STIFFNESS. DATE OF IMPLANTATION: (B)(6) 2011, DATE OF REVISION: (B)(6) 2020, (RIGHT KNEE). TREATMENT: REVISION OF TIBIAL TRAY, FEMUR, AND TIBIAL INSERT.

    Patient problems: Muscular Rigidity; Pain

    MAUDE report 11261262 ↗

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

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Sources and updates

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