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LCS 1278-16-000Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS TIBIAL INSERT ROTATING PLATFORM BRIDGING BEARING SM+/STD 15mm · Class 3 · Implant

All models of LCS (45)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295020288), received between Dec 16, 2021 and Dec 16, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Naturally Worn” (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

  • Naturally Worn1
  • Unintended Movement1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionDec 16, 2021Naturally Worn; Unintended Movement; Naturally Worn; Unintended Movement

    ADDITIONAL INFORMATION RECEIVED INDICATED THAT THE INSERT HAS ROTATED AND THE REVISION SURGERY SHOULD BE PERFORMED.

    Patient problems: Insufficient Information

    MAUDE report 13017670 ↗

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Sources and updates

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