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ADVANCE® KFSCNP3RRecalls & reported problems

Microport Orthopedics Inc. · ADVANCE® STEMMED MEDIAL PIVOT NONPOROUS FEMORAL SIZE 3 RIGHT · 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 M684KFSCNP3R1), received between Dec 26, 2019 and Dec 26, 2019 — classified as 1 injury.

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

  • Break1
  • Insufficient Device Problem Information1

Patient problems

  • Bone Fracture(s)1
  • No Information1

Recent adverse event reports

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

  • InjuryDec 26, 2019Break; Insufficient Device Problem Information; Break; Insufficient Device Problem Information

    ALLEGEDLY, PATIENT UNDERWENT PRIMARY SURGERY, WHICH WAS LATER REVISED ON (B)(6) 2009 DUE TO UNKNOWN REASONS. REVISED THE REVISION COMPONENTS ON (B)(6) 2019 DUE TO FEMORAL IMPLANT FRACTURE. (B)(4).

    Patient problems: Bone Fracture(s); No Information

    MAUDE report 9519333 ↗

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.