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LCS COMPLETE AOX 1294-18-415Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE TIBIAL INSERT ROTATING PLATFORM RP AOX STD 15mm · Class 3 · Implant

All models of LCS COMPLETE AOX (10)

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 10603295024170), received between Apr 8, 2020 and Apr 8, 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

  • 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.

  • InjuryApr 8, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    LEFT TOTAL KNEE DONE AT (B)(6) ON (B)(6) 2020. PATIENT DEVELOPED AN INFECTION SO REMOVED POLY AND PERFORMED AN I&D. THE PATIENT EXHIBITED SOME SYMPTOMS OF COVID19, SUCH AS A COUGH AND SLIGHT FEVER, HOWEVER CHEST XRAY SEEMED CLEAR. ALL COVID19 PRECAUTIONS WERE ADHERED TO DURING REVISION SURGERY.

    Patient problems: No Code Available; Unspecified Infection

    MAUDE report 9940073 ↗

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Sources and updates

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