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ADVANCE® KFTCPC5LRecalls & reported problems

Microport Orthopedics Inc. · ADVANCE® PRIMARY FEMORAL SIZE 5 LEFT POROUS · 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 M684KFTCPC5L1), received between Dec 9, 2020 and Dec 9, 2020 — 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

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.

  • InjuryDec 9, 2020Break; Break

    ALLEGEDLY, MEDIAL CONDYLE OF THE FEMORAL COMPONENT FRACTURED CAUSING PAIN AND INSTABILITY. ADDITIONAL INFORMATION RECEIVED ON 11/20/2020: REASON OF INCIDENT, IMPLANT YEAR, INCIDENT DATE, REVISION DATE, PATIENT INFORMATION. LEFT KNEE.

    Patient problems: No Information

    MAUDE report 10976170 ↗

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.