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GENESIS II 71422032Recalls & reported problems

Smith & Nephew, Inc. · GENESIS II CRUCIATE RETAINING HYDROXYAPATITE POROUS FEMORAL SIZE 6 RIGHT · Class 2 · Implant

All models of GENESIS II (462)

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 03596010496249), received between Apr 24, 2019 and Apr 24, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Unstable” (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

  • Unstable1

Patient problems

  • Injury1

Recent adverse event reports

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

  • InjuryApr 24, 2019Unstable; Unstable

    IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO FLEXION INSTABILITY AND TIGHTNESS LATERALLY. TIBIA, PATELLA, INSERT, FEMORAL WERE EXPLANTED AND REPLACED WITH COMPETITORS DEVICES.

    Patient problems: Injury

    MAUDE report 8547346 ↗

Other PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices →

Sources and updates

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