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LCS COMPLETE 1294-26-063Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE DISTAL AUGMENT 5mm LG 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 10603295025191), received between May 8, 2020 and May 8, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of Osseointegration” (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 Osseointegration1

Patient problems

  • Inadequate Osseointegration1
  • No Code Available1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryMay 8, 2020Loss of Osseointegration; Loss of Osseointegration

    THE PATIENT WAS REVISED DUE TO POSSIBLE INFECTION AND LOOSENING OF THE FEMORAL AUGMENTS AT THE BONE TO IMPLANT INTERFACE. DOI: UNKNOWN. DOR: (B)(6) 2020; LEFT KNEE.

    Patient problems: Inadequate Osseointegration; No Code Available; Unspecified Infection

    MAUDE report 10038972 ↗

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Sources and updates

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