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SIGMA LCS HIGH PERFORMANCE 9505-02-025Recalls & reported problems

Depuy (Ireland) · SIGMA LCS HIGH PERFORMANCE MBT CENTRAL DRILL CEMENTED · Class 1

All models of SIGMA LCS HIGH PERFORMANCE (6)

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 10603295227458), received between Jan 22, 2018 and Jan 22, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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

  • Device-Device Incompatibility1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionJan 22, 2018Device-Device Incompatibility; Device-Device Incompatibility

    IT WAS REPORTED THAT THE INSTRUMENT WON'T ENGAGE PROPERLY AND CREATING WEAR. NO SURGICAL DELAY.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7209104 ↗

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Sources and updates

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