Skip to content

LCS COMPLETE 1294-42-050Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE MODULAR FEMORAL CEMENTED STD+ 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 10603295026174), received between Mar 5, 2018 and Mar 5, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • Ambulation or Postural Difficulties1
  • Bone Fracture(s)1
  • Hematoma1
  • Joint Disorder1
  • Limited Mobility Of The Implanted Joint1
  • Pain1
  • Swelling1
  • Weakness1

Recent adverse event reports

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

  • InjuryMar 5, 2018Fracture; Fracture

    FRACTURE OF A LCS REVISION COMPONENT (FEMORAL, POSTERIOR-CONDYLE).

    Patient problems: Ambulation or Postural Difficulties; Bone Fracture(s); Hematoma; Joint Disorder; Limited Mobility Of The Implanted Joint; Pain; Swelling; Weakness

    MAUDE report 7312718 ↗

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

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

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page