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ADVANCE® KIPS2312Recalls & reported problems

Microport Orthopedics Inc. · ADVANCE® II POST STAB TIBIAL INSERT SIZE 3 12mm · 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 M684KIPS23121), received between Jun 29, 2020 and Jun 29, 2020 — classified as 1 injury.

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

  • Unstable1

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.

  • InjuryJun 29, 2020Unstable; Unstable

    ALLEGEDLY, PATIENT WAS REVISED DUE TO INSTABILITY. COMPONENT NOT REVISED: ADVANCE ONLAY ALL POLY PATELLA 35MM TRIPEG PRODUCT ID: KPONTP35 LOT ID: 1759570. REVISION NJR NUMBER: 4387320. PRIMARY ASA: P3 - INCAPACITATING SYSTEMIC DISEASE.

    Patient problems: No Information

    MAUDE report 10206269 ↗

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

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Sources and updates

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