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ADVANCE® KFSCNP4RRecalls & reported problems

Microport Orthopedics Inc. · ADVANCE® STEMMED MEDIAL PIVOT NONPOROUS FEMORAL SIZE 4 RIGHT · Class 2 · Implant

Data updated Oct 13, 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 M684KFSCNP4R1), received between Aug 22, 2019 and Aug 22, 2019 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Loose or Intermittent Connection1

Patient problems

  • No Information1

Recent adverse event reports

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

  • InjuryAug 22, 2019Loose or Intermittent Connection; Loose or Intermittent Connection

    ALLEGEDLY THE PATIENT WAS REVISED DUE TO COMPONENT ARE LOOSE. ALL COMPONENTS CAME OUT.

    Patient problems: No Information

    MAUDE report 8922867 ↗

Other Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer devices

All Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer devices →

Sources and updates

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