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LCS COMPLETE 1294-02-070Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE PRIMARY FEMORAL CEMENTED LRG+ LEFT · 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 10603295021650), received between Jan 6, 2020 and Jan 6, 2020 — 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 16, 2026.

Most reported problems

Device problems

  • Loss of or Failure to Bond1

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.

  • InjuryJan 6, 2020Loss of or Failure to Bond; Loss of or Failure to Bond

    THE PATIENT WAS REVISED TO ADDRESS PAIN AND LOOSENING OF THE FEMORAL AND TIBIAL COMPONENTS AT THE CEMENT TO IMPLANT INTERFACE. COMPETITOR CEMENT WAS USED. DOI: 2018; DOR: (B)(6), 2019; LEFT KNEE.

    Patient problems: No Code Available; Pain

    MAUDE report 9553583 ↗

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Sources and updates

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