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SIGMA 1024-08-600Recalls & reported problems

Depuy (Ireland) · SIGMA HIGH PERFORMANCE PARTIAL KNEE FEMORAL UNICONDYLAR CEMENTED SIZE 6 RM/LL · Class 2 · Implant

All models of SIGMA (380)

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 10603295001829), received between Sep 13, 2022 and Sep 13, 2022 — 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

  • Pain1

Recent adverse event reports

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

  • InjurySep 13, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    REMOVAL OF UNI-KNEE IMPLANT CONSTRUCTS. PATIENT HAD UNI-COMPARTMENTAL KNEE REPLACEMENT ON THE RIGHT MEDIAL SIDE IN 2021. POST OPERATIVELY THE PATIENT EXPERIENCED CONSISTENT MEDIAL COMPARTMENT KNEE PAIN. THEREFORE A DECISION WAS MADE TO REMOVE THE UNI-COMPARTMENTAL CONSTRUCT AND IMPLANT A FULL ATTUNE PRIMARY KNEE CONSTRUCT. DOI: UNKNOWN, DOR: (B)(6) 2022, RIGHT KNEE.

    Patient problems: Pain

    MAUDE report 15411043 ↗

Other PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER devices

All PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER devices →

Sources and updates

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