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LCS COMPLETE 1294-24-322Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE TIBIAL INSERT ROTATING PLATFORM VVC REVISION 22.5mm MED · 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 10603295024620), received between Sep 22, 2020 and Sep 22, 2020 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Inflammation1
  • Limited Mobility Of The Implanted Joint1
  • No Code Available1
  • Pain1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjurySep 22, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    ADDITIONAL INFORMATION RECEIVED CONFIRMING THE INFECTION. IT WAS STATED THAT THERE WAS A CULTURE GROWN FROM THE RETRIEVED SPECIMENS THAT ARE LIKELY TO HAVE LEAD TO THE COMPONENT LOOSENING (BUG TYPE NOT CONFIRMED).

    Patient problems: Inflammation; Limited Mobility Of The Implanted Joint; No Code Available; Pain; Unspecified Infection

    MAUDE report 10567459 ↗

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Sources and updates

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