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Advance KTSLFM50Recalls & reported problems

Microport Orthopedics Inc. · ADVANCE® BIOFOAM® TIBIA BASE W/O SCREWHOLES SIZE 5 · 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 M684KTSLFM501), received between Jan 14, 2020 and Jan 14, 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

  • No Information1

Recent adverse event reports

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

  • InjuryJan 14, 2020Loss of Osseointegration; Loss of Osseointegration

    ALLEGEDLY MECHANICAL LOOSENING OF TIBIA. COMPONENT NOT REVISED: ADVANCE PRIMARY FEMORAL - PRODUCT ID KFTCPC5R LOT NO: NI. ADDITIONAL INFORMATION: RIGHT KNEE PATELLA FROM STRYKER.

    Patient problems: No Information

    MAUDE report 9586426 ↗

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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