Skip to content

ADVANCE® KIPS2510Recalls & reported problems

Microport Orthopedics Inc. · ADVANCE® II POST STAB TIBIAL INSERT SIZE 5 10mm · 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 M684KIPS25101), received between Jul 28, 2021 and Jul 28, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Material Too Rigid or Stiff” (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

  • Material Too Rigid or Stiff1

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.

  • InjuryJul 28, 2021Material Too Rigid or Stiff

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

    Patient problems: Loss of Range of Motion

    MAUDE report 12240240 ↗

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

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

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page