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LCS COMPLETE 1294-27-061Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE POSTERIOR AUGMENT 10mm LG · 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 10603295025399), received between Jun 19, 2018 and Jun 19, 2018 — 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 18, 2026.

Most reported problems

Device problems

  • Loss of or Failure to Bond1

Patient problems

  • No Consequences Or Impact To Patient1
  • Not Applicable1

Recent adverse event reports

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

  • InjuryJun 19, 2018Loss of or Failure to Bond; Loss of or Failure to Bond

    REVISION TOTAL KNEE REPLACEMENT, DR. (B)(6), (B)(6) 2018. REVISION OF REVISION LCS TKR DUE TO FEMORAL LOOSENING, TIBIA REMAINED INSTITU. PATIENT INITIALS: (B)(6), MALE (B)(6). UNKNOWN JRN: LCS COMP RP LARGE 12.5MM REVISION. UNKNOWN JRN: LARGE FEMUR LEFT REVISION. UNKNOWN: JRN: 115 X 20 MM UNCEMENTED TIBIAL STEM.

    Patient problems: No Consequences Or Impact To Patient; Not Applicable

    MAUDE report 7613082 ↗

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

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Sources and updates

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