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ADVANCE® KIPS2414Recalls & reported problems

Microport Orthopedics Inc. · ADVANCE® II POST STAB TIBIAL INSERT SIZE 4 14mm · 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 M684KIPS24141), received between Jun 26, 2019 and Jun 26, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Malposition of Device” (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

  • Malposition of Device1

Patient problems

  • Loss of Range of Motion1

Recent adverse event reports

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

  • InjuryJun 26, 2019Malposition of Device; Malposition of Device

    ALLEGEDLY THE PATIENT WAS REVISED DUE TO MALALIGNMENT; STIFFNESS. REVISION NJR NUMBER: (B)(4), SIDE: R. PRIMARY ASA: P2-MILD DISEASE NOT INCAPACITATING.

    Patient problems: Loss of Range of Motion

    MAUDE report 8736692 ↗

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

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

Sources and updates

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