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ADVANCE® KITC210RRecalls & reported problems

Microport Orthopedics Inc. · ADVANCE® I MEDIAL PIVOT INSERT SIZE 2 RIGHT 10mm · 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 M684KITC210R1), received between Mar 12, 2020 and Mar 12, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1

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.

  • InjuryMar 12, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY, LOOKS LIKE AN ADVANCE 1 KNEE. DR. POMPO IN CONNECTICUT WANTS TO REMOVE THE SCREWS IN THE TIB TRAY AND SWAP THE POLY. BUT HE HASNT MADE CLEAR YET WHETHER OR NOT HE WANTS TO REPLACE THE TIB TRAY. TRYING TO GET A GRASP ON NECESSARY INSTRUMENTATION.

    Patient problems: No Information

    MAUDE report 9826240 ↗

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.