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ADVANCE® KSP18140Recalls & reported problems

Microport Orthopedics Inc. · ADVANCE® CANAL FILLING STEM EXTENSION 19mm X 140mm · Class 2 · Implant

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 M684KSP181401), received between Jan 21, 2021 and Jan 21, 2021 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Loss of Osseointegration1
  • Unstable1

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.

  • InjuryJan 21, 2021Unstable; Loss of Osseointegration; Unstable; Loss of Osseointegration

    ALLEGEDLY, THE PATIENT SUFFERED PAIN AND INSTABILITY; LOOSENING OF FEMUR AND STEM. (LEFT KNEE) COMPONENT NOT REVISED: ADVANCE® II MODULAR TITANIUM TIBIAL BASE SZ 4 STD / PRODUCT ID: KTTINP40 / LOT NUMBER: 085268636.

    Patient problems: Pain

    MAUDE report 11210659 ↗

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

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

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.