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ADVANCE® KFSCNP1LRecalls & reported problems

Microport Orthopedics Inc. · ADVANCE® STEMMED MEDIAL PIVOT NONPOROUS FEMORAL SIZE 1 LEFT · Class 2 · Implant

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 M684KFSCNP1L1), received between Aug 5, 2020 and Aug 5, 2020 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available1

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.

  • InjuryAug 5, 2020Appropriate Device Problem Term/Code Not Available

    ALLEGEDLY, PATIENT WAS REVISED DUE TO PAIN AND POLY SWAP TO A THICKER SIZE.

    Patient problems: Pain

    MAUDE report 10371273 ↗

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

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

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.