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Advance KTSSFM40Recalls & reported problems

Microport Orthopedics Inc. · ADVANCE® BIOFOAM® TIBIA BASE W/ SCREWHOLES SIZE 4 · Class 2 · Implant

All models of ADVANCE (147)

Data updated Oct 16, 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 M684KTSSFM401), received between Mar 10, 2020 and Mar 10, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of Osseointegration” (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 16, 2026.

Most reported problems

Device problems

  • Loss of Osseointegration1

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.

  • InjuryMar 10, 2020Loss of Osseointegration; Loss of Osseointegration

    ALLEGEDLY, PATIENT HAS PAIN ON RIGHT KNEE AND ON FILM THERE APPEARS TO BE SIGNS OF IMPLANT LOOSENING. ALL IMPLANTS WERE REMOVED AND REPLACED WITH ODC IMPLANTS.

    Patient problems: Pain

    MAUDE report 9811983 ↗

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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