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LCS COMPLETE 1294-09-770Recalls & reported problems

Depuy (Ireland) · LCS COMPLETE Metal Backed Patella CEMENTED LRG+ · Class 3 · Implant

All models of LCS COMPLETE (18)

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 10603295022749), received between May 7, 2018 and May 7, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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

  • Loose or Intermittent Connection1

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.

  • InjuryMay 7, 2018Loose or Intermittent Connection; Loose or Intermittent Connection

    PATIENT HAD KNEE REVISION FOR ASEPTIC LOOSENING OF ALL COMPONENTS.

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

    MAUDE report 7490085 ↗

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Sources and updates

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